WNT10A, Wnt family member 10A, 80326

N. diseases: 136; N. variants: 41
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7349332
rs7349332
0.807 0.080 2 218891661 intron variant C/G;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs74333950
rs74333950
0.807 0.080 2 218881570 intron variant T/G snv 0.13
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016