Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs769540300 0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs75012854 0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs774847933 0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 5
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4