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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6