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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs4906902 0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs12912233 0.851 0.120 15 60974897 intron variant C/T snv 0.38 5