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rs10770141

From SNPedia

Orientationplus
Stabilizedplus
Make rs10770141(A;A)
Make rs10770141(A;G)
Make rs10770141(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2172610
GeneMIR4686, TH
is asnp
is mentioned by
dbSNPrs10770141
ebirs10770141
HLIrs10770141
Exacrs10770141
Varsomers10770141
Maprs10770141
PheGenIrs10770141
hapmaprs10770141
1000 genomesrs10770141
hgdprs10770141
ensemblrs10770141
gopubmedrs10770141
geneviewrs10770141
scholarrs10770141
googlers10770141
pharmgkbrs10770141
gwascentralrs10770141
openSNPrs10770141
23andMers10770141
23andMe allrs10770141
SNP Nexus

SNPshotrs10770141
SNPdbers10770141
MSV3drs10770141
GWAS Ctlgrs10770141
GMAF0.3604
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19958792] Association study between a functional polymorphism of tyrosine hydroxylase gene promoter and personality traits in healthy subjects


[PMID 20571875OA-icon.png] Human Tyrosine Hydroxylase Natural Allelic Variation: Influence on Autonomic Function and Hypertension


[PMID 17717598OA-icon.png] Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.


[PMID 18180394OA-icon.png] Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.


[PMID 23246742] Association of monoamine-synthesizing genes with the depression tendency and personality in chronic fatigue syndrome patients.