rs1444768
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1444768(C;C) |
| Make rs1444768(C;T) |
| Make rs1444768(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 124205075 |
| Gene | KALRN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1444768 |
| dbSNP (classic) | rs1444768 |
| ClinGen | rs1444768 |
| ebi | rs1444768 |
| HLI | rs1444768 |
| Exac | rs1444768 |
| Gnomad | rs1444768 |
| Varsome | rs1444768 |
| LitVar | rs1444768 |
| Map | rs1444768 |
| PheGenI | rs1444768 |
| Biobank | rs1444768 |
| 1000 genomes | rs1444768 |
| hgdp | rs1444768 |
| ensembl | rs1444768 |
| geneview | rs1444768 |
| scholar | rs1444768 |
| rs1444768 | |
| pharmgkb | rs1444768 |
| gwascentral | rs1444768 |
| openSNP | rs1444768 |
| 23andMe | rs1444768 |
| SNPshot | rs1444768 |
| SNPdbe | rs1444768 |
| MSV3d | rs1444768 |
| GWAS Ctlg | rs1444768 |
| GMAF | 0.4656 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19706030
] Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking
[PMID 17357071] Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
