Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10