rs12373237
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12373237(A;A) |
| Make rs12373237(A;G) |
| Make rs12373237(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 23845972 |
| Gene | LAMA3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12373237 |
| dbSNP (classic) | rs12373237 |
| ClinGen | rs12373237 |
| ebi | rs12373237 |
| HLI | rs12373237 |
| Exac | rs12373237 |
| Gnomad | rs12373237 |
| Varsome | rs12373237 |
| LitVar | rs12373237 |
| Map | rs12373237 |
| PheGenI | rs12373237 |
| Biobank | rs12373237 |
| 1000 genomes | rs12373237 |
| hgdp | rs12373237 |
| ensembl | rs12373237 |
| geneview | rs12373237 |
| scholar | rs12373237 |
| rs12373237 | |
| pharmgkb | rs12373237 |
| gwascentral | rs12373237 |
| openSNP | rs12373237 |
| 23andMe | rs12373237 |
| SNPshot | rs12373237 |
| SNPdbe | rs12373237 |
| MSV3d | rs12373237 |
| GWAS Ctlg | rs12373237 |
| GMAF | 0.3765 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20036365] Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals
[PMID 20372818] Genetic risk for myocardial infarction in Japanese individuals with or without chronic kidney disease
