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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs79105258 12 111280427 intron variant C/A;T snv 24
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs668459 6 139514552 intron variant C/T snv 0.51 5
rs7178615 15 66576734 intergenic variant A/G snv 0.66 2