rs9806699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9806699(A;A) |
| Make rs9806699(A;G) |
| Make rs9806699(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 45448194 |
| Gene | LOC105376714 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9806699 |
| dbSNP (classic) | rs9806699 |
| ClinGen | rs9806699 |
| ebi | rs9806699 |
| HLI | rs9806699 |
| Exac | rs9806699 |
| Gnomad | rs9806699 |
| Varsome | rs9806699 |
| LitVar | rs9806699 |
| Map | rs9806699 |
| PheGenI | rs9806699 |
| Biobank | rs9806699 |
| 1000 genomes | rs9806699 |
| hgdp | rs9806699 |
| ensembl | rs9806699 |
| geneview | rs9806699 |
| scholar | rs9806699 |
| rs9806699 | |
| pharmgkb | rs9806699 |
| gwascentral | rs9806699 |
| openSNP | rs9806699 |
| 23andMe | rs9806699 |
| SNPshot | rs9806699 |
| SNPdbe | rs9806699 |
| MSV3d | rs9806699 |
| GWAS Ctlg | rs9806699 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25863251
] GATM Polymorphism Associated with the Risk for Statin-Induced Myopathy Does Not Replicate in Case-Control Analysis of 715 Dyslipidemic Individuals
[PMID 33150478] Correlation between single-nucleotide polymorphisms and statin-induced myopathy: a mixed-effects model meta-analysis.
