Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs10847697 0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs13385731 0.882 0.200 2 33476823 intron variant T/C snv 6.3E-02 3