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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1799913 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5