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: rs879255280
rs879255280
0.701 0.200 7 129206557 missense variant C/T snv
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder
Skin and Connective Tissue Diseases 0.700 0