Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs4148217 0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 11
rs4299376 0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs4245791 0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs2072183 0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 6
rs4953023 0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 6
rs6756629 0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 5