Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 57
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 44
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50