Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs757075712 0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 15
rs1131692245 0.925 0.160 19 35844109 missense variant C/T snv 7
rs1049305 0.925 0.160 7 30924207 3 prime UTR variant G/C snv 0.52 4
rs113090017 0.882 0.200 12 100532538 stop gained C/A;G;T snv 4.0E-06; 2.4E-05 4
rs3741559 1.000 0.160 12 49951193 splice region variant G/A snv 0.20 0.17 3
rs467323 12 49955982 3 prime UTR variant C/G;T snv 2