rs2210327
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2210327(A;A) |
| Make rs2210327(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 18109237 |
| Gene | ADAMTSL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2210327 |
| dbSNP (classic) | rs2210327 |
| ClinGen | rs2210327 |
| ebi | rs2210327 |
| HLI | rs2210327 |
| Exac | rs2210327 |
| Gnomad | rs2210327 |
| Varsome | rs2210327 |
| LitVar | rs2210327 |
| Map | rs2210327 |
| PheGenI | rs2210327 |
| Biobank | rs2210327 |
| 1000 genomes | rs2210327 |
| hgdp | rs2210327 |
| ensembl | rs2210327 |
| geneview | rs2210327 |
| scholar | rs2210327 |
| rs2210327 | |
| pharmgkb | rs2210327 |
| gwascentral | rs2210327 |
| openSNP | rs2210327 |
| 23andMe | rs2210327 |
| SNPshot | rs2210327 |
| SNPdbe | rs2210327 |
| MSV3d | rs2210327 |
| GWAS Ctlg | rs2210327 |
| GMAF | 0.1019 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20445134 ]
|
| Trait | Heart failure |
| Title | The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium |
| Risk Allele | |
| P-val | 7E-7 |
| Odds Ratio | 3.14 [0.99-10.00] |
