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
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs2072621 0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7