rs3737965
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs3737965(C;T) |
| Make rs3737965(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11806394 |
| Gene | CLCN6, MTHFR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3737965 |
| dbSNP (classic) | rs3737965 |
| ClinGen | rs3737965 |
| ebi | rs3737965 |
| HLI | rs3737965 |
| Exac | rs3737965 |
| Gnomad | rs3737965 |
| Varsome | rs3737965 |
| LitVar | rs3737965 |
| Map | rs3737965 |
| PheGenI | rs3737965 |
| Biobank | rs3737965 |
| 1000 genomes | rs3737965 |
| hgdp | rs3737965 |
| ensembl | rs3737965 |
| geneview | rs3737965 |
| scholar | rs3737965 |
| rs3737965 | |
| pharmgkb | rs3737965 |
| gwascentral | rs3737965 |
| openSNP | rs3737965 |
| 23andMe | rs3737965 |
| SNPshot | rs3737965 |
| SNPdbe | rs3737965 |
| MSV3d | rs3737965 |
| GWAS Ctlg | rs3737965 |
| GMAF | 0.05188 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26740945
] The rs3737964 single-nucleotide polymorphism of the chloride channel-6 gene as a risk factor for coronary heart disease.
