Have questions? Visit https://www.reddit.com/r/SNPedia

rs10770140

From SNPedia

Orientationplus
Stabilizedplus
Make rs10770140(C;C)
Make rs10770140(C;T)
Make rs10770140(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2172367
GeneMIR4686, TH
is asnp
is mentioned by
dbSNPrs10770140
ebirs10770140
HLIrs10770140
Exacrs10770140
Varsomers10770140
Maprs10770140
PheGenIrs10770140
hapmaprs10770140
1000 genomesrs10770140
hgdprs10770140
ensemblrs10770140
gopubmedrs10770140
geneviewrs10770140
scholarrs10770140
googlers10770140
pharmgkbrs10770140
gwascentralrs10770140
openSNPrs10770140
23andMers10770140
23andMe allrs10770140
SNP Nexus

SNPshotrs10770140
SNPdbers10770140
MSV3drs10770140
GWAS Ctlgrs10770140
GMAF0.3549
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20571875OA-icon.png] Human Tyrosine Hydroxylase Natural Allelic Variation: Influence on Autonomic Function and Hypertension

[PMID 19604093OA-icon.png] Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.