Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs12203582
IL17F
0.827 0.120 6 52240759 intron variant G/A;T snv 7
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4