Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
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
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174