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
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs9399136 6 135081201 intron variant T/C snv 0.18 4
rs218264 4 54542708 intergenic variant A/G;T snv 3