Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs5516 0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs140598 0.827 0.160 15 48487333 missense variant G/A;C snv 3.2E-02 5
rs1465567 0.882 0.040 5 38370435 missense variant T/C snv 0.20 0.25 3