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
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
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
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
rs28364997 0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs16976358 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs1460808228 0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs12456492 0.882 0.080 18 43093415 intron variant A/G snv 0.33 3
rs7122539
PC
0.925 0.040 11 66895260 intron variant G/A snv 0.43 2