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: rs3096697
rs3096697
0.882 0.200 6 32166733 missense variant G/A snv 0.16 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs3130347
rs3130347
1.000 0.040 6 32166879 intron variant T/C snv 0.15 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010