TH, tyrosine hydroxylase, 7054

N. diseases: 321; N. variants: 71
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10770141
rs10770141
1.000 0.120 11 2172610 upstream gene variant A/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1213545562
rs1213545562
1.000 0.080 11 2166984 synonymous variant G/A snv 9.6E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1384915680
rs1384915680
1.000 0.080 11 2166903 synonymous variant G/A snv 4.3E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2005 2005