Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1042114 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1079597 0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs1126671 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs2234918 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs1042363 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs149775276 0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 2
rs779838446 0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 2