rs2302765
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs2302765(A;G) |
| Make rs2302765(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 7447656 |
| Gene | CHRNB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2302765 |
| dbSNP (classic) | rs2302765 |
| ClinGen | rs2302765 |
| ebi | rs2302765 |
| HLI | rs2302765 |
| Exac | rs2302765 |
| Gnomad | rs2302765 |
| Varsome | rs2302765 |
| LitVar | rs2302765 |
| Map | rs2302765 |
| PheGenI | rs2302765 |
| Biobank | rs2302765 |
| 1000 genomes | rs2302765 |
| hgdp | rs2302765 |
| ensembl | rs2302765 |
| geneview | rs2302765 |
| scholar | rs2302765 |
| rs2302765 | |
| pharmgkb | rs2302765 |
| gwascentral | rs2302765 |
| openSNP | rs2302765 |
| 23andMe | rs2302765 |
| SNPshot | rs2302765 |
| SNPdbe | rs2302765 |
| MSV3d | rs2302765 |
| GWAS Ctlg | rs2302765 |
| GMAF | 0.1731 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Variations in this snp have been linked to nicotine dependence [1]
[PMID 17373692
] No evidence for association between 19 cholinergic genes and bipolar disorder.
[PMID 19259974] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
| ClinVar | |
|---|---|
| Risk | rs2302765(G;G) |
| Alt | rs2302765(G;G) |
| Reference | Rs2302765(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Congenital Myasthenic Syndrome |
| Variation | info |
| Gene | CHRNB1 |
| CLNDBN | not specified Congenital Myasthenic Syndrome, Dominant/Recessive |
| Reversed | 1 |
| HGVS | NC_000017.10:g.7350975T>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000116725.3, RCV000397260.1, |
