Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10511729 0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11896604 0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144