Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2073837
DBH-AS1 ; DBH
9 133657806 intron variant G/A snv 0.31 1
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs7118900
ANKK1
11 113396099 missense variant G/A snv 0.25 0.25 1
rs772527880
AGFG1
2 227531108 missense variant G/A snv 4.0E-06 1
rs963549
OPRK1
8 53229264 synonymous variant C/T snv 0.17 0.24 1
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480