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 24
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 5