rs7548522
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs7548522(C;T) |
| Make rs7548522(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 239835325 |
| Gene | CHRM3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7548522 |
| dbSNP (classic) | rs7548522 |
| ClinGen | rs7548522 |
| ebi | rs7548522 |
| HLI | rs7548522 |
| Exac | rs7548522 |
| Gnomad | rs7548522 |
| Varsome | rs7548522 |
| LitVar | rs7548522 |
| Map | rs7548522 |
| PheGenI | rs7548522 |
| Biobank | rs7548522 |
| 1000 genomes | rs7548522 |
| hgdp | rs7548522 |
| ensembl | rs7548522 |
| geneview | rs7548522 |
| scholar | rs7548522 |
| rs7548522 | |
| pharmgkb | rs7548522 |
| gwascentral | rs7548522 |
| openSNP | rs7548522 |
| 23andMe | rs7548522 |
| SNPshot | rs7548522 |
| SNPdbe | rs7548522 |
| MSV3d | rs7548522 |
| GWAS Ctlg | rs7548522 |
| GMAF | 0.0404 |
| Max Magnitude | 0 |
| ? | (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.
