Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2107538 0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs1800451 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9