Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 7
rs147233090 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs2603151 4 68502154 downstream gene variant A/G snv 0.63 2