Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs4072111 0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11 16
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242