Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs2235749 0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs1042114 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1079597 0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs2234918 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5