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
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs1264350
LINC00243
0.925 0.160 6 30828768 intron variant T/C snv 9.4E-02 2
rs2858870
HLA-DRB1
0.851 0.280 6 32604474 intergenic variant T/A;C snv 2
rs3094061 0.925 0.160 6 30353412 downstream gene variant A/C;T snv 2
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38 2