Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs660118 0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205