Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs8679 0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs1805404 0.882 0.200 1 226402257 missense variant G/A;C snv 0.22; 4.0E-06 3
rs1805414 0.925 0.080 1 226385663 synonymous variant A/G snv 0.43 0.42 2
rs2230484 0.925 0.080 1 226383066 missense variant G/A snv 3.7E-03 3.3E-03 2
rs4653734 0.925 0.080 1 226407688 intron variant C/A;G snv 2
rs907187 0.925 0.080 1 226407946 5 prime UTR variant C/G;T snv 0.21; 4.1E-06 2