Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs6065904 1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs1106076 1.000 0.080 7 5581212 regulatory region variant C/A;G snv 2
rs12305135 1.000 0.080 12 130150660 non coding transcript exon variant T/C snv 6.8E-02 2
rs10812227 1.000 0.080 9 2548556 intron variant C/G;T snv 2
rs201815520 1.000 0.080 6 77463302 synonymous variant G/A snv 1.4E-05 1