Disease: Vitiligo
Source: GWASDB ×
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 13
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs130065
CCHCR1
0.925 0.120 6 31154723 missense variant G/A snv 0.15 0.16 2