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

rs7548522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7548522(C;T)
Make rs7548522(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position239835325
GeneCHRM3
is asnp
is mentioned by
dbSNPrs7548522
dbSNP (classic)rs7548522
ClinGenrs7548522
ebirs7548522
HLIrs7548522
Exacrs7548522
Gnomadrs7548522
Varsomers7548522
LitVarrs7548522
Maprs7548522
PheGenIrs7548522
Biobankrs7548522
1000 genomesrs7548522
hgdprs7548522
ensemblrs7548522
geneviewrs7548522
scholarrs7548522
googlers7548522
pharmgkbrs7548522
gwascentralrs7548522
openSNPrs7548522
23andMers7548522
SNPshotrs7548522
SNPdbers7548522
MSV3drs7548522
GWAS Ctlgrs7548522
GMAF0.0404
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 21450750] Potential association of muscarinic receptor 3 gene variants with primary Sjogren's syndrome

[PMID 31747477] Evaluation of Muscarinic Acetylcholine Receptor Type 3 Gene Polymorphisms in Patients with Primary Biliary Cholangitis and Primary Sclerosing Cholangitis.