Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23
rs121908552 0.763 0.160 17 63964587 missense variant C/A;G;T snv 4.0E-06 14
rs80338962 0.742 0.240 17 63941508 missense variant T/C snv 13
rs80338957 0.776 0.160 17 63957427 missense variant G/A snv 11
rs80338958 0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 9
rs121908547 0.790 0.160 17 63943825 missense variant G/A snv 4.0E-06 7
rs527236148 0.790 0.160 17 63971201 missense variant G/A snv 7.0E-06 7
rs80338792 0.827 0.160 17 63943846 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 7
rs886041805 0.790 0.160 17 63941506 missense variant C/A;T snv 7
rs121908545 0.851 0.160 17 63941939 missense variant C/A;G;T snv 5
rs80338784 0.851 0.160 17 63959278 missense variant C/T snv 8.0E-06 4
rs80338788 0.851 0.160 17 63959269 missense variant C/A;T snv 4.0E-06; 1.2E-05 4
rs121908548 0.851 0.160 17 63941517 missense variant C/T snv 4
rs80338789 0.851 0.160 17 63947091 missense variant C/T snv 1.4E-05 4
rs80338785 0.851 0.160 17 63959270 missense variant G/A;C;T snv 4
rs80338956 0.882 0.160 17 63957460 missense variant A/G snv 3
rs121908544 0.882 0.160 17 63941940 missense variant G/A;T snv 3
rs121908551 0.882 0.160 17 63944708 missense variant C/T snv 7.0E-06 3
rs527236150 0.882 0.160 17 63947082 missense variant C/T snv 3
rs121908556 0.925 0.160 17 63957515 missense variant G/A;C snv 1.2E-05 2
rs864622785 0.925 0.160 17 63964600 missense variant A/C snv 2
rs1567816549 0.925 0.160 17 63941982 missense variant A/G snv 2
rs763893717 0.925 0.160 17 63941840 missense variant G/A;T snv 2
rs80338959 0.925 0.160 17 63943036 missense variant T/C snv 2
rs80338960 0.925 0.160 17 63943006 missense variant T/C snv 4.0E-06 2