rs9925481
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9925481(C;C) |
| Make rs9925481(C;T) |
| Make rs9925481(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11003622 |
| Gene | CLEC16A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9925481 |
| dbSNP (classic) | rs9925481 |
| ClinGen | rs9925481 |
| ebi | rs9925481 |
| HLI | rs9925481 |
| Exac | rs9925481 |
| Gnomad | rs9925481 |
| Varsome | rs9925481 |
| LitVar | rs9925481 |
| Map | rs9925481 |
| PheGenI | rs9925481 |
| Biobank | rs9925481 |
| 1000 genomes | rs9925481 |
| hgdp | rs9925481 |
| ensembl | rs9925481 |
| geneview | rs9925481 |
| scholar | rs9925481 |
| rs9925481 | |
| pharmgkb | rs9925481 |
| gwascentral | rs9925481 |
| openSNP | rs9925481 |
| 23andMe | rs9925481 |
| SNPshot | rs9925481 |
| SNPdbe | rs9925481 |
| MSV3d | rs9925481 |
| GWAS Ctlg | rs9925481 |
| GMAF | 0.1162 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 19787205] Association of genetic variants with myocardial infarction in individuals with or without hypertension or diabetes mellitus
[PMID 20036365] Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals
[PMID 20043139] Association of genetic variants with ischemic stroke in Japanese individuals with or without metabolic syndrome
[PMID 20372818] Genetic risk for myocardial infarction in Japanese individuals with or without chronic kidney disease
