Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2524123
rs2524123
HLA-B ; LINC02571 ; LOC112267902
0.925 0.040 6 31297537 intron variant T/C snv 0.34
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010