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rs2070762

From SNPedia

Orientationminus
Stabilizedminus
Make rs2070762(C;C)
Make rs2070762(C;T)
Make rs2070762(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2165105
GeneTH
is asnp
is mentioned by
dbSNPrs2070762
ebirs2070762
HLIrs2070762
Exacrs2070762
Varsomers2070762
Maprs2070762
PheGenIrs2070762
hapmaprs2070762
1000 genomesrs2070762
hgdprs2070762
ensemblrs2070762
gopubmedrs2070762
geneviewrs2070762
scholarrs2070762
googlers2070762
pharmgkbrs2070762
gwascentralrs2070762
openSNPrs2070762
23andMers2070762
23andMe allrs2070762
SNP Nexus

SNPshotrs2070762
SNPdbers2070762
MSV3drs2070762
GWAS Ctlgrs2070762
GMAF0.4325
Max Magnitude
? (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 19772578OA-icon.png] 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 19673036OA-icon.png] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.


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


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


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 19956106OA-icon.png] 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