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
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3