Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7195386 0.925 0.120 16 24567137 splice region variant T/A;C snv 0.56 2
rs72755233 1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs7534091 1 118321993 intergenic variant A/G snv 0.23 2
rs76895963 1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs76929617 12 120429995 intergenic variant A/G snv 3.7E-02 2
rs7740107 1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs7826312 8 32542597 intron variant T/C snv 0.57 2
rs9880211 3 136388707 intron variant G/A snv 0.19 2