Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs121908117 0.708 0.440 3 48466707 missense variant G/A snv 17
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14