rs11089788
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11089788(A;A) |
| Make rs11089788(A;C) |
| Make rs11089788(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36355056 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11089788 |
| dbSNP (classic) | rs11089788 |
| ClinGen | rs11089788 |
| ebi | rs11089788 |
| HLI | rs11089788 |
| Exac | rs11089788 |
| Gnomad | rs11089788 |
| Varsome | rs11089788 |
| LitVar | rs11089788 |
| Map | rs11089788 |
| PheGenI | rs11089788 |
| Biobank | rs11089788 |
| 1000 genomes | rs11089788 |
| hgdp | rs11089788 |
| ensembl | rs11089788 |
| geneview | rs11089788 |
| scholar | rs11089788 |
| rs11089788 | |
| pharmgkb | rs11089788 |
| gwascentral | rs11089788 |
| openSNP | rs11089788 |
| 23andMe | rs11089788 |
| SNPshot | rs11089788 |
| SNPdbe | rs11089788 |
| MSV3d | rs11089788 |
| GWAS Ctlg | rs11089788 |
| GMAF | 0.3549 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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[PMID 19387472] Genome-wide linkage analysis of serum creatinine in three isolated European populations
[PMID 21245129] Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese
[PMID 20124285
] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
[PMID 23516419] Epistatic Role of the MYH9/APOL1 Region on Familial Hematuria Genes
