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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2070074 0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 12
rs7561460 1.000 0.040 2 102000742 intron variant T/C snv 0.43 2