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
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7