Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3859501 0.882 0.120 19 53788157 non coding transcript exon variant A/C snv 0.43 3