Disease: Vitiligo
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 5
rs78645479
FOXD3-AS1 ; FOXD3
0.851 0.120 1 63322631 5 prime UTR variant C/G;T snv 4