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: rs1481318368
rs1481318368
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.090 1.000 9 2013 2020
dbSNP: rs6356
rs6356
0.827 0.240 11 2169721 missense variant C/T snv 0.43 0.32
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.040 0.500 4 1996 2018
dbSNP: rs121917763
rs121917763
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 1998 1998