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
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
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs678849 0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4