rs9972882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9972882(A;A) |
| Make rs9972882(A;C) |
| Make rs9972882(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 39651445 |
| Gene | STARD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9972882 |
| dbSNP (classic) | rs9972882 |
| ClinGen | rs9972882 |
| ebi | rs9972882 |
| HLI | rs9972882 |
| Exac | rs9972882 |
| Gnomad | rs9972882 |
| Varsome | rs9972882 |
| LitVar | rs9972882 |
| Map | rs9972882 |
| PheGenI | rs9972882 |
| Biobank | rs9972882 |
| 1000 genomes | rs9972882 |
| hgdp | rs9972882 |
| ensembl | rs9972882 |
| geneview | rs9972882 |
| scholar | rs9972882 |
| rs9972882 | |
| pharmgkb | rs9972882 |
| gwascentral | rs9972882 |
| openSNP | rs9972882 |
| 23andMe | rs9972882 |
| SNPshot | rs9972882 |
| SNPdbe | rs9972882 |
| MSV3d | rs9972882 |
| GWAS Ctlg | rs9972882 |
| GMAF | 0.3949 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 24291029] Association analysis of ERBB2 amplicon genetic polymorphisms and STARD3 expression with risk of gastric cancer in the Chinese population
[PMID 30108155
] Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
