rs464218
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs464218(C;C) |
| Make rs464218(C;T) |
| Make rs464218(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 109313684 |
| Gene | SORT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs464218 |
| dbSNP (classic) | rs464218 |
| ClinGen | rs464218 |
| ebi | rs464218 |
| HLI | rs464218 |
| Exac | rs464218 |
| Gnomad | rs464218 |
| Varsome | rs464218 |
| LitVar | rs464218 |
| Map | rs464218 |
| PheGenI | rs464218 |
| Biobank | rs464218 |
| 1000 genomes | rs464218 |
| hgdp | rs464218 |
| ensembl | rs464218 |
| geneview | rs464218 |
| scholar | rs464218 |
| rs464218 | |
| pharmgkb | rs464218 |
| gwascentral | rs464218 |
| openSNP | rs464218 |
| 23andMe | rs464218 |
| SNPshot | rs464218 |
| SNPdbe | rs464218 |
| MSV3d | rs464218 |
| GWAS Ctlg | rs464218 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26464717
] Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke
