rs1324694
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs1324694(C;T) |
| Make rs1324694(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 100186688 |
| Gene | ERLIN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1324694 |
| dbSNP (classic) | rs1324694 |
| ClinGen | rs1324694 |
| ebi | rs1324694 |
| HLI | rs1324694 |
| Exac | rs1324694 |
| Gnomad | rs1324694 |
| Varsome | rs1324694 |
| LitVar | rs1324694 |
| Map | rs1324694 |
| PheGenI | rs1324694 |
| Biobank | rs1324694 |
| 1000 genomes | rs1324694 |
| hgdp | rs1324694 |
| ensembl | rs1324694 |
| geneview | rs1324694 |
| scholar | rs1324694 |
| rs1324694 | |
| pharmgkb | rs1324694 |
| gwascentral | rs1324694 |
| openSNP | rs1324694 |
| 23andMe | rs1324694 |
| SNPshot | rs1324694 |
| SNPdbe | rs1324694 |
| MSV3d | rs1324694 |
| GWAS Ctlg | rs1324694 |
| GMAF | 0.07254 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals
