Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1182 0.790 0.160 9 129813781 3 prime UTR variant C/A snv 0.17 9
rs587776983 0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
rs1801968 0.827 0.040 9 129818622 missense variant C/G;T snv 0.13; 4.0E-06 7