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 92
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23