Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs3194051 0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64