rs9838682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9838682(A;A) |
| Make rs9838682(A;G) |
| Make rs9838682(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 30349375 |
| Gene | LOC101927995 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9838682 |
| dbSNP (classic) | rs9838682 |
| ClinGen | rs9838682 |
| ebi | rs9838682 |
| HLI | rs9838682 |
| Exac | rs9838682 |
| Gnomad | rs9838682 |
| Varsome | rs9838682 |
| LitVar | rs9838682 |
| Map | rs9838682 |
| PheGenI | rs9838682 |
| Biobank | rs9838682 |
| 1000 genomes | rs9838682 |
| hgdp | rs9838682 |
| ensembl | rs9838682 |
| geneview | rs9838682 |
| scholar | rs9838682 |
| rs9838682 | |
| pharmgkb | rs9838682 |
| gwascentral | rs9838682 |
| openSNP | rs9838682 |
| 23andMe | rs9838682 |
| SNPshot | rs9838682 |
| SNPdbe | rs9838682 |
| MSV3d | rs9838682 |
| GWAS Ctlg | rs9838682 |
| GMAF | 0.4504 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 19959123
] Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease
[PMID 19654303] Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
