Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs2571445 0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs4766578 0.851 0.200 12 111466567 intron variant T/A snv 0.66 4