rs6995588
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs6995588(C;T) |
| Make rs6995588(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 60091338 |
| Gene | LOC105375861 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6995588 |
| dbSNP (classic) | rs6995588 |
| ClinGen | rs6995588 |
| ebi | rs6995588 |
| HLI | rs6995588 |
| Exac | rs6995588 |
| Gnomad | rs6995588 |
| Varsome | rs6995588 |
| LitVar | rs6995588 |
| Map | rs6995588 |
| PheGenI | rs6995588 |
| Biobank | rs6995588 |
| 1000 genomes | rs6995588 |
| hgdp | rs6995588 |
| ensembl | rs6995588 |
| geneview | rs6995588 |
| scholar | rs6995588 |
| rs6995588 | |
| pharmgkb | rs6995588 |
| gwascentral | rs6995588 |
| openSNP | rs6995588 |
| 23andMe | rs6995588 |
| SNPshot | rs6995588 |
| SNPdbe | rs6995588 |
| MSV3d | rs6995588 |
| GWAS Ctlg | rs6995588 |
| GMAF | 0.1084 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21348951 ]
|
| Trait | |
| Title | Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
