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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs3771829 0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs1805502 0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs324650 0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs1034936 0.882 0.080 12 2551994 intron variant C/T snv 0.61 3
rs12898460 0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251 0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs1701137 0.882 0.080 17 572682 intron variant C/T snv 0.50 3
rs3771856 0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57 3
rs10051667 0.925 0.080 5 161471322 intron variant T/C snv 0.12 2
rs1805247 0.925 0.080 12 13563041 synonymous variant A/G snv 0.13 0.17 2
rs2727943 0.925 0.080 3 1856289 intergenic variant T/A;C snv 2