Disease: Vitiligo
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12