rs2070762

Orientation

minus

Stabilized

minus

Make rs2070762(C;C)

Make rs2070762(C;T)

Make rs2070762(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2165105

Gene

TH

is a	snp
is	mentioned by
dbSNP	rs2070762
dbSNP (classic)	rs2070762
ClinGen	rs2070762
ebi	rs2070762
HLI	rs2070762
Exac	rs2070762
Gnomad	rs2070762
Varsome	rs2070762
LitVar	rs2070762
Map	rs2070762
PheGenI	rs2070762
Biobank	rs2070762
1000 genomes	rs2070762
hgdp	rs2070762
ensembl	rs2070762
geneview	rs2070762
scholar	rs2070762
google	rs2070762
pharmgkb	rs2070762
gwascentral	rs2070762
openSNP	rs2070762
23andMe	rs2070762
SNPshot	rs2070762
SNPdbe	rs2070762
MSV3d	rs2070762
GWAS Ctlg	rs2070762

GMAF

0.4325

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 18208403] association with essential hypertension . Functional analysis showed that the C allele of rs2070762 functioned as an enhancer in the absence of binding by unidentified transcriptional repressor(s)

[PMID 19772578] Two-stage case-control association study of dopamine-related genes and migraine

[PMID 16636198] Association study with 33 single-nucleotide polymorphisms in 11 candidate genes for hypertension in Chinese.

[PMID 19673036] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

[PMID 19693267] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.

[PMID 19772600] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.

[PMID 19956101] Overview of the Rapid Response data.

[PMID 19956106] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.

[PMID 24275212] The role of tyrosine hydroxylase gene variants in suicide attempt in schizophrenia