Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs3020450 0.807 0.200 14 64301584 splice region variant C/A;T snv 10