Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9