Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 10
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 110
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 20
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs753955 0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 9
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214