Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2228671 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs562556 0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8