Bovine genetic disease and major gene testing
Making the most of your herd through trait-specific testing

Introducing genes that cause high mortality or embryonic loss are costly to producers, while introducing genes that produce a positive effect on the animals production can be a good way to increase profits. Testing for both desirable and undesirable genes is a cost-effective way to ensure you are getting the most genetic potential from your herd. Weatherbys Scientific is introducing a number of these tests to the market to ensure your herd maintains and elevates its genetic potential. The tests we offer are listed below by specific trait and by the breeds they are known to be in, so you can tailor your decisions based on your specific animal or herd’s need.

Traits by breed and type
Genetic traits by breed
Angus  Trait Abbreviation Product Code
Developmental Duplication Variants  (Unwanted) DD GXL0188_DD
Neuropathic hydrocephalus Variants  (Lethal-Embryo) NH GXL0188_NH
Alpha Mannosidosis_961 Variants  (Lethal) AM_961 GXL0188_AM_961
Ayrshire
Trimethylaminuria Variants  (Milk) FMO3 GXL0188_FMO3
Belgian Blue
Arthrogryposis with Cleft Palate Variants  (Lethal) ACP GXL0188_ACP
Congenital Muscular Dystonia 1 Variants  (Lethal) CMD1 GXL0188_CMD1
Congenital Muscular Dystonia 2 Variants  (Lethal) CMD2 GXL0188_CMD2
Dwarfism, Belgium Blue Variants  (Unwanted) RNF11 GXL0188_RNF11
Crooked Tail Syndrome delAG Variants  (Unwanted) CTS_delAG GXL0188_CTS_delAG
Belted Galloway
Alpha Mannosidosis_662 Variants  (Lethal) AM_662 GXL0188_AM_662
Hypotrichosis_HEPHL1 Variants  (Unwanted) HY_HEPHL1 GXL0188_HY_HEPHL1
PMEL17_delTTC Variants  (Colour) PMEL17_delTTC GXL0188_PMEL17_delTTC
Tibial Hemimelia_Improver Variants  (Lethal) TH_Imp GXL0188_TH_Imp
Blonde d’Aquitaine
Protoporphyria Variants  (Unwanted) PROTO GXL0188_PROTO
Brangus
Alpha Mannosidosis_961 Variants  (Lethal) AM_961 GXL0188_AM_961
Brown Swiss
Axonopathy Variants  (Unwanted) AX GXL0188_AX
Spinal Muscular Atrophy Variants  (Unwanted) SMA GXL0188_SMA
Bovine Spinal Dysmyelination Variants  (Lethal) BSD GXL0188_BSD
Arachnomelia Syndrome_SUOX Variants  (Lethal) ARAC_SUOX GXL0188_ARAC_SUOX
Charolais
Silver Char Dilutor_1 Variants  (Colour) PMEL17_64G_A GXL0188_PMEL17_64G_A
Chianina
Pseudomyotonia_c491G>A Variants  (Unwanted) PMT_164 GXL0188_PMT_164
Dahomey
Bulldog Dwarfism 1 Variants  (Lethal-Embryo) BD1 GXL0188_BD1
Devon
Neuronal ceroid lipofuscinosis Variants  (Lethal) NCL GXL0188_NCL
Dexter
Dun Dexter Variants  (Colour) DUN GXL0188_DUN
Bulldog Dwarfism 1 Variants  (Lethal-Embryo) BD1 GXL0188_BD1
Dutch Improved Red and White
Congenital Muscular Dystonia 1 Variants  (Lethal) CMD1 GXL0188_CMD1
Finnish Ayrshire
Ptosis, retarded growth and intelect Variants  (Lethal) PIRM GXL0188_PIRM
Fleckvieh
Bovine Hereditary Zinc Deficiency Variants  (Unwanted) BHZD GXL0188_BHZD
Idiopathic Male subfertility Variants  (unwanted) IDMS GXL0188_IDMS
Arachnomelia Syndrome_MOCS1 Variants  (Lethal) ARAS_MOCS1 GXL0188_ARAS_MOCS1
Fleckvieh Haplotype 4 (embryonic loss), Variants  (Lethal-Embryo) FH4 GXL0188_FH4
Friesian
Polled Friesian_1909396D2 Variants  (Beneficial) POLL_F GXL0188_POLL_F
Polled Friesian_51D Variants  (Beneficial) POLL_F_51D GXL0188_POLL_F_51D
Polled Friesian_C1655463T Variants  (Beneficial) POLL_F_C1655463T GXL0188_POLL_F_C1655463T
Polled Friesian_G1654405A Variants  (Beneficial) POLL_F_G1654405A GXL0188_POLL_F_G1654405A
Gelbvieh
Myostatin L64P Variants  (Meat) MYO_L64P GXL0188_MYO_L64P
Glanrind
Myostatin L64P Variants  (Meat) MYO_L64P GXL0188_MYO_L64P
Hereford
Cardiomyopathy and woolly hair coat syndrome Variants  (Lethal) CWH GXL0188_CWH
Congenital Myoclonus Variants  (Unwanted) CM GXL0188_CM
Idiopathic Epilepsy Variants  (Lethal) IE GXL0188_IE
Hypotrichosis_KRT71 Variants  (Unwanted) HY_KRT71 GXL0188_HY_KRT71
Maple Syrup Urine Disease_Hereford Variants  (Lethal) MSU_HER GXL0188_MSU_HER
PMEL17_1835C_A Variants  (Colour) PMEL17_1835C_A GXL0188_PMEL17_1835C_A
Highland
PMEL17_delTTC Variants  (Colour) PMEL17_delTTC GXL0188_PMEL17_delTTC
Holstein
Axonopathy Variants  (Unwanted) AX GXL0188_AX
Bovine Leukocyte Adhesion Deficiency Variants  (Unwanted) BLAD GXL0188_BLAD
Brachyspina Variants  (Lethal-Embryo) BY GXL0188_BY
Complex Vertebral Malformation Variants  (Lethal-Embryo) CVM GXL0188_CVM
Deficiency of Uridine Monophosphate Synthase Variants  (Lethal-Embryo) DUMPS GXL0188_DUMPS
Ehlers Danlos Syndrome-Holstein Variant Variants  (Unwanted) EDS_Hol GXL0188_EDS_Hol
Yellow milk fat Variants  (Milk) YMF GXL0188_YMF
Dominant red Variants  (Colour) HDR GXL0188_HDR
Holstein Haplotype 1 Variants  (Lethal-Embryo) HH1 GXL0188_HH1
Holstein Haplotype 3 Variants  (Lethal-Embryo) HH3 GXL0188_HH3
Holstein Haplotype 4 Variants  (Lethal-Embryo) HH4 GXL0188_HH4
Hypotrichosis Steaked_ERCC6L Variants  (Unwanted) HY_ERCC6L GXL0188_HY_ERCC6L
Hypotrichosis Steaked_TSR2 Variants  (Unwanted) HY_TSR2 GXL0188_HY_TSR2
Mulefoot NG1621KC Variants  (Unwanted) MF_NG1621KC GXL0188_MF_NG1621KC
Polled Friesian_1909396D2 Variants  (Beneficial) POLL_F GXL0188_POLL_F
Polled Friesian_51D Variants  (Beneficial) POLL_F_51D GXL0188_POLL_F_51D
Polled Friesian_C1655463T Variants  (Beneficial) POLL_F_C1655463T GXL0188_POLL_F_C1655463T
Polled Friesian_G1654405A Variants  (Beneficial) POLL_F_G1654405A GXL0188_POLL_F_G1654405A
STAT1 Variants  (Unwanted) STAT1 GXL0188_STAT1
STAT3_19069 Variants  (Unwanted) STAT3_19069 GXL0188_STAT3_19069
STAT3_25402 Variants  (Unwanted) STAT3_25402 GXL0188_STAT3_25402
STAT5_13244 Variants  (Unwanted) STAT5_13244 GXL0188_STAT5_13244
STAT5_13319 Variants  (Unwanted) STAT5_13319 GXL0188_STAT5_13319
STAT5_13516 Variants  (Unwanted) STAT5_13516 GXL0188_STAT5_13516
Japanese Black
Perinatal weak calf syndrome Variants  (Lethal) PWCS GXL0188_PWCS
Spherocytosis Variants  (Unwanted) SP GXL0188_SP
Chediak_Higashi syndrome Variants  (Unwanted) CHS GXL0188_CHS
Jersey
Yellow milk fat Variants  (Milk) YMF GXL0188_YMF
Jersey Haplotype 1 Variants  (Lethal-Embryo) JH1 GXL0188_JH1
Limousin
Protoporphyria Variants  (Unwanted) PROTO GXL0188_PROTO
Limpurger
Myostatin L64P Variants  (Meat) MYO_L64P GXL0188_MYO_L64P
Montbéliarde
Montbéliarde Haplotype 2 Variants  (Lethal-Embryo) MH2 GXL0188_MH2
Multiple breeds
ABCG2 Variants  (Milk) ABCG2 GXL0188_ABCG2
Citrullinemia Variants  (Lethal) CT GXL0188_CT
Polled Celtic Variants  (Beneficial) POLL_C GXL0188_POLL_C
AcylCoA:Diacylglycerol Acyltransferase Variants  (Milk) DGAT1 GXL0188_DGAT1
Calpain1 316 Variants  (Meat) CAPN1_316 GXL0188_CAPN1_316
Calpain1 4751 Variants  (Meat) CAPN1_4751 GXL0188_CAPN1_4751
Calpain1 530 Variants  (Meat) CAPN1_530 GXL0188_CAPN1_530
Calpastatin 282 Variants  (Meat) CAST_282 GXL0188_CAST_282
Calpastatin 2870 Variants  (Meat) CAST_2870 GXL0188_CAST_2870
Calpastatin 2959 Variants  (Meat) CAST_2959 GXL0188_CAST_2959
Casein Beta A2 Variants  (Milk) CSN2_A2 GXL0188_CSN2_A2
Casein Beta A3 Variants  (Milk) CSN2_A3 GXL0188_CSN2_A3
Chondrodysplasia 1 Variants  (Lethal) CD1 GXL0188_CD1
Coat colour Black gene E, extension Variants  (Colour) MC1R_ED GXL0188_MC1R_ED
Coat colour Red factor e Variants  (Colour) MC1R_e GXL0188_MC1R_e
Growth Hormone Receptor F279Y Variants  (Milk) GHR_F279Y GXL0188_GHR_F279Y
Growth Hormone_2141 Variants  (Milk) GH_2141 GXL0188_GH_2141
Growth Hormone_2291 Variants  (Milk) GH_2291 GXL0188_GH_2291
Kappa Casein B variant Variants  (Milk) CSN3_B_Varaint GXL0188_CSN3_B_Varaint
Kappa Casein E variant Variants  (Milk) CSN3_E_Varaint GXL0188_CSN3_E_Varaint
Mulefoot G907R Variants  (Unwanted) MF_G907R GXL0188_MF_G907R
Myostatin C313Y Variants  (Meat) MYO_C313Y GXL0188_MYO_C313Y
Myostatin D182N Variants  (Meat) MYO_D182N GXL0188_MYO_D182N
Myostatin E226X Variants  (Meat) MYO_E226X GXL0188_MYO_E226X
Myostatin E291X Variants  (Meat) MYO_E291X GXL0188_MYO_E291X
Myostatin F94L Variants  (Meat) MYO_F94L GXL0188_MYO_F94L
Myostatin nt267 Variants  (Meat) MYO_nt267 GXL0188_MYO_nt267
Myostatin nt324 Variants  (Meat) MYO_nt324 GXL0188_MYO_nt324
Myostatin nt414 Variants  (Meat) MYO_nt414 GXL0188_MYO_nt414
Myostatin nt419 Variants  (Meat) MYO_nt419 GXL0188_MYO_nt419
Myostatin nt748_78 Variants  (Meat) MYO_nt748_78 GXL0188_MYO_nt748_78
Myostatin nt821DEL11 Variants  (Meat) MYO_nt821 GXL0188_MYO_nt821
Myostatin Q204X Variants  (Meat) MYO_Q204X GXL0188_MYO_Q204X
Myostatin S105C Variants  (Meat) MYO_S105C GXL0188_MYO_S105C
White Heifer Disease/Roan_coat_colour Variants  (Colour) WFD_Roan GXL0188_WFD_Roan
Progressive Degenerative Myeloencephalopathy Variants  (Unwanted) Weaver GXL0188_Weaver
Murray Grey
Alpha Mannosidosis_961 Variants  (Lethal) AM_961 GXL0188_AM_961
Nordic Red dairy
RNASEH2B_del Variants  (Lethal) RNASEH2B_del GXL0188_RNASEH2B_del
Pezzata Rossa
Hypotrichosis Steaked_ERCC6L Variants  (Unwanted) HY_ERCC6L GXL0188_HY_ERCC6L
Hypotrichosis Steaked_TSR2 Variants  (Unwanted) HY_TSR2 GXL0188_HY_TSR2
Red Angus
Alpha Mannosidosis_961 Variants  (Lethal) AM_961 GXL0188_AM_961
Red Danish Dairy
Bovine Spinal Dysmyelination Variants  (Lethal) BSD GXL0188_BSD
Romagnola
Paunch Calf Syndrome Variants  (Lethal) PCS GXL0188_PCS
Pseudomyotonia_c491G>A Variants  (Unwanted) PMT_164 GXL0188_PMT_164
Pseudomyotonia_c632G>T Variants  (Unwanted) PMT_211 GXL0188_PMT_211
Pseudomyotonia_c857G>T Variants  (Unwanted) PMT_284 GXL0188_PMT_284
Rotes Hohenvieh
Dystrophic Epidermolysis Bullosa Variants  (Unwanted) DEB GXL0188_DEB
Salers
Beta Mannosidosis Variants  (Lethal) BM GXL0188_BM
Shorthorn
Maple Syrup Urine Disease_Shorthorn Variants  (Lethal) MSU_SH GXL0188_MSU_SH
Tibial Hemimelia_Improver Variants  (Lethal) TH_Imp GXL0188_TH_Imp
Simmental
Thrombopathia Variants  (Unwanted) THR GXL0188_THR
Arachnomelia Syndrome_MOCS1 Variants  (Lethal) ARAS_MOCS1 GXL0188_ARAS_MOCS1
Mulefoot G1199S Variants  (Unwanted) MF_G1199S GXL0188_MF_G1199S
PMEL17_delTTC Variants  (Colour) PMEL17_delTTC GXL0188_PMEL17_delTTC
Tibial Hemimelia_Improver Variants  (Lethal) TH_Imp GXL0188_TH_Imp
Swedish Red and White
Trimethylaminuria Variants  (Milk) FMO3 GXL0188_FMO3
Tyrolean Grey
Axonopathy Variants  (Unwanted) AX GXL0188_AX
Vorderwald
Dystrophic Epidermolysis Bullosa Variants  (Unwanted) DEB GXL0188_DEB
Wagyu
Factor XI deficiency Wagyu Variants  (Unwanted) FXI_WA GXL0188_FXI_WA
Genetic traits by type
Beneficial  Trait Abbreviation   Product Code 
Polled Celtic Variants  (Beneficial) POLL_C GXL0188_POLL_C
Polled Friesian_1909396D2 Variants  (Beneficial) POLL_F GXL0188_POLL_F
Polled Friesian_51D Variants  (Beneficial) POLL_F_51D GXL0188_POLL_F_51D
Polled Friesian_C1655463T Variants  (Beneficial) POLL_F_C1655463T GXL0188_POLL_F_C1655463T
Polled Friesian_G1654405A Variants  (Beneficial) POLL_F_G1654405A GXL0188_POLL_F_G1654405A
Colour
Coat colour Black gene E, extension Variants  (Colour) MC1R_ED GXL0188_MC1R_ED
Coat colour Red factor e Variants  (Colour) MC1R_e GXL0188_MC1R_e
Dominant red Variants  (Colour) HDR GXL0188_HDR
Dun Dexter Variants  (Colour) DUN GXL0188_DUN
PMEL17_1835C_A Variants  (Colour) PMEL17_1835C_A GXL0188_PMEL17_1835C_A
PMEL17_delTTC Variants  (Colour) PMEL17_delTTC GXL0188_PMEL17_delTTC
Silver Char Dilutor_1 Variants  (Colour) PMEL17_64G_A GXL0188_PMEL17_64G_A
White Heifer Disease/Roan_coat_colour Variants  (Colour) WFD_Roan GXL0188_WFD_Roan
Lethal
Alpha Mannosidosis_662 Variants  (Lethal) AM_662 GXL0188_AM_662
Alpha Mannosidosis_961 Variants  (Lethal) AM_961 GXL0188_AM_961
Arachnomelia Syndrome_MOCS1 Variants  (Lethal) ARAS_MOCS1 GXL0188_ARAS_MOCS1
Arachnomelia Syndrome_SUOX Variants  (Lethal) ARAC_SUOX GXL0188_ARAC_SUOX
Arthrogryposis with Cleft Palate Variants  (Lethal) ACP GXL0188_ACP
Beta Mannosidosis Variants  (Lethal) BM GXL0188_BM
Bovine Spinal Dysmyelination Variants  (Lethal) BSD GXL0188_BSD
Cardiomyopathy and woolly hair coat syndrome Variants  (Lethal) CWH GXL0188_CWH
Chondrodysplasia 1 Variants  (Lethal) CD1 GXL0188_CD1
Citrullinemia Variants  (Lethal) CT GXL0188_CT
Congenital Muscular Dystonia 1 Variants  (Lethal) CMD1 GXL0188_CMD1
Congenital Muscular Dystonia 2 Variants  (Lethal) CMD2 GXL0188_CMD2
Idiopathic Epilepsy Variants  (Lethal) IE GXL0188_IE
Maple Syrup Urine Disease_Hereford Variants  (Lethal) MSU_HER GXL0188_MSU_HER
Maple Syrup Urine Disease_Shorthorn Variants  (Lethal) MSU_SH GXL0188_MSU_SH
Neuronal ceroid lipofuscinosis Variants  (Lethal) NCL GXL0188_NCL
Paunch Calf Syndrome Variants  (Lethal) PCS GXL0188_PCS
Perinatal weak calf syndrome Variants  (Lethal) PWCS GXL0188_PWCS
RNASEH2B_del Variants  (Lethal) RNASEH2B_del GXL0188_RNASEH2B_del
Tibial Hemimelia_Improver Variants  (Lethal) TH_Imp GXL0188_TH_Imp
Ptosis, retarded growth and intelect Variants  (Lethal) PIRM GXL0188_PIRM
Lethal-Embryo
Brachyspina Variants  (Lethal-Embryo) BY GXL0188_BY
Bulldog Dwarfism 1 Variants  (Lethal-Embryo) BD1 GXL0188_BD1
Complex Vertebral Malformation Variants  (Lethal-Embryo) CVM GXL0188_CVM
Deficiency of Uridine Monophosphate Synthase Variants  (Lethal-Embryo) DUMPS GXL0188_DUMPS
Fleckvieh Haplotype 4 (embryonic loss), Variants  (Lethal-Embryo) FH4 GXL0188_FH4
Holstein Haplotype 1 Variants  (Lethal-Embryo) HH1 GXL0188_HH1
Holstein Haplotype 3 Variants  (Lethal-Embryo) HH3 GXL0188_HH3
Holstein Haplotype 4 Variants  (Lethal-Embryo) HH4 GXL0188_HH4
Jersey Haplotype 1 Variants  (Lethal-Embryo) JH1 GXL0188_JH1
Montbéliarde Haplotype 2 Variants  (Lethal-Embryo) MH2 GXL0188_MH2
Neuropathic hydrocephalus Variants  (Lethal-Embryo) NH GXL0188_NH
Meat
Calpain1 316 Variants  (Meat) CAPN1_316 GXL0188_CAPN1_316
Calpain1 4751 Variants  (Meat) CAPN1_4751 GXL0188_CAPN1_4751
Calpain1 530 Variants  (Meat) CAPN1_530 GXL0188_CAPN1_530
Calpastatin 282 Variants  (Meat) CAST_282 GXL0188_CAST_282
Calpastatin 2870 Variants  (Meat) CAST_2870 GXL0188_CAST_2870
Calpastatin 2959 Variants  (Meat) CAST_2959 GXL0188_CAST_2959
Myostatin C313Y Variants  (Meat) MYO_C313Y GXL0188_MYO_C313Y
Myostatin D182N Variants  (Meat) MYO_D182N GXL0188_MYO_D182N
Myostatin E226X Variants  (Meat) MYO_E226X GXL0188_MYO_E226X
Myostatin E291X Variants  (Meat) MYO_E291X GXL0188_MYO_E291X
Myostatin F94L Variants  (Meat) MYO_F94L GXL0188_MYO_F94L
Myostatin L64P Variants  (Meat) MYO_L64P GXL0188_MYO_L64P
Myostatin nt267 Variants  (Meat) MYO_nt267 GXL0188_MYO_nt267
Myostatin nt324 Variants  (Meat) MYO_nt324 GXL0188_MYO_nt324
Myostatin nt414 Variants  (Meat) MYO_nt414 GXL0188_MYO_nt414
Myostatin nt419 Variants  (Meat) MYO_nt419 GXL0188_MYO_nt419
Myostatin nt748_78 Variants  (Meat) MYO_nt748_78 GXL0188_MYO_nt748_78
Myostatin nt821DEL11 Variants  (Meat) MYO_nt821 GXL0188_MYO_nt821
Myostatin Q204X Variants  (Meat) MYO_Q204X GXL0188_MYO_Q204X
Myostatin S105C Variants  (Meat) MYO_S105C GXL0188_MYO_S105C
Milk
ABCG2 Variants  (Milk) ABCG2 GXL0188_ABCG2
AcylCoA:Diacylglycerol Acyltransferase Variants  (Milk) DGAT1 GXL0188_DGAT1
Casein Beta A2 Variants  (Milk) CSN2_A2 GXL0188_CSN2_A2
Casein Beta A3 Variants  (Milk) CSN2_A3 GXL0188_CSN2_A3
Growth Hormone Receptor F279Y Variants  (Milk) GHR_F279Y GXL0188_GHR_F279Y
Growth Hormone_2141 Variants  (Milk) GH_2141 GXL0188_GH_2141
Growth Hormone_2291 Variants  (Milk) GH_2291 GXL0188_GH_2291
Kappa Casein B variant Variants  (Milk) CSN3_B_Varaint GXL0188_CSN3_B_Varaint
Kappa Casein E variant Variants  (Milk) CSN3_E_Varaint GXL0188_CSN3_E_Varaint
Yellow milk fat Variants  (Milk) YMF GXL0188_YMF
Trimethylaminuria Variants  (Milk) FMO3 GXL0188_FMO3
Unwanted
Axonopathy Variants  (Unwanted) AX GXL0188_AX
Bovine Hereditary Zinc Deficiency Variants  (Unwanted) BHZD GXL0188_BHZD
Bovine Leukocyte Adhesion Deficiency Variants  (Unwanted) BLAD GXL0188_BLAD
Chediak_Higashi syndrome Variants  (Unwanted) CHS GXL0188_CHS
Congenital Myoclonus Variants  (Unwanted) CM GXL0188_CM
Crooked Tail Syndrome delAG Variants  (Unwanted) CTS_delAG GXL0188_CTS_delAG
Developmental Duplication Variants  (Unwanted) DD GXL0188_DD
Dwarfism, Belgium Blue Variants  (Unwanted) RNF11 GXL0188_RNF11
Dystrophic Epidermolysis Bullosa Variants  (Unwanted) DEB GXL0188_DEB
Ehlers Danlos Syndrome-Holstein Variant Variants  (Unwanted) EDS_Hol GXL0188_EDS_Hol
Factor XI deficiency Wagyu Variants  (Unwanted) FXI_WA GXL0188_FXI_WA
Hypotrichosis Steaked_ERCC6L Variants  (Unwanted) HY_ERCC6L GXL0188_HY_ERCC6L
Hypotrichosis Steaked_TSR2 Variants  (Unwanted) HY_TSR2 GXL0188_HY_TSR2
Hypotrichosis_HEPHL1 Variants  (Unwanted) HY_HEPHL1 GXL0188_HY_HEPHL1
Hypotrichosis_KRT71 Variants  (Unwanted) HY_KRT71 GXL0188_HY_KRT71
Idiopathic Male subfertility Variants  (unwanted) IDMS GXL0188_IDMS
Mulefoot G1199S Variants  (Unwanted) MF_G1199S GXL0188_MF_G1199S
Mulefoot G907R Variants  (Unwanted) MF_G907R GXL0188_MF_G907R
Mulefoot NG1621KC Variants  (Unwanted) MF_NG1621KC GXL0188_MF_NG1621KC
Protoporphyria Variants  (Unwanted) PROTO GXL0188_PROTO
Pseudomyotonia_c491G>A Variants  (Unwanted) PMT_164 GXL0188_PMT_164
Pseudomyotonia_c632G>T Variants  (Unwanted) PMT_211 GXL0188_PMT_211
Pseudomyotonia_c857G>T Variants  (Unwanted) PMT_284 GXL0188_PMT_284
Spherocytosis Variants  (Unwanted) SP GXL0188_SP
Spinal Muscular Atrophy Variants  (Unwanted) SMA GXL0188_SMA
STAT1 Variants  (Unwanted) STAT1 GXL0188_STAT1
STAT3_19069 Variants  (Unwanted) STAT3_19069 GXL0188_STAT3_19069
STAT3_25402 Variants  (Unwanted) STAT3_25402 GXL0188_STAT3_25402
STAT5_13244 Variants  (Unwanted) STAT5_13244 GXL0188_STAT5_13244
STAT5_13319 Variants  (Unwanted) STAT5_13319 GXL0188_STAT5_13319
STAT5_13516 Variants  (Unwanted) STAT5_13516 GXL0188_STAT5_13516
Thrombopathia Variants  (Unwanted) THR GXL0188_THR
Progressive Degenerative Myeloencephalopathy Variants  (Unwanted) Weaver GXL0188_Weaver