Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80356616 0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356624 0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs80356618 0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs80356625 0.827 0.280 11 17387491 missense variant G/A snv 6
rs80356637 0.851 0.240 11 17470119 missense variant A/C;G snv 4
rs80356615 0.851 0.240 11 17387934 missense variant C/T snv 4
rs80356617 0.882 0.160 11 17387916 missense variant A/C snv 3
rs80356620 0.882 0.160 11 17387593 missense variant T/G snv 3
rs387906783 0.925 0.160 11 17387913 missense variant A/G;T snv 2