Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs3741380 1.000 0.040 11 65581592 missense variant G/A snv 0.48 0.48 3