rs6601299
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs6601299(C;T) |
| Make rs6601299(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 9327181 |
| Gene | LOC157273 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6601299 |
| dbSNP (classic) | rs6601299 |
| ClinGen | rs6601299 |
| ebi | rs6601299 |
| HLI | rs6601299 |
| Exac | rs6601299 |
| Gnomad | rs6601299 |
| Varsome | rs6601299 |
| LitVar | rs6601299 |
| Map | rs6601299 |
| PheGenI | rs6601299 |
| Biobank | rs6601299 |
| 1000 genomes | rs6601299 |
| hgdp | rs6601299 |
| ensembl | rs6601299 |
| geneview | rs6601299 |
| scholar | rs6601299 |
| rs6601299 | |
| pharmgkb | rs6601299 |
| gwascentral | rs6601299 |
| openSNP | rs6601299 |
| 23andMe | rs6601299 |
| SNPshot | rs6601299 |
| SNPdbe | rs6601299 |
| MSV3d | rs6601299 |
| GWAS Ctlg | rs6601299 |
| GMAF | 0.0955 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21347282 ]
|
| Trait | |
| Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
| Risk Allele | T |
| P-val | 1E-8 |
| Odds Ratio | 0.1407 [0.09-0.19] SD decrease |
