rs5750248
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs5750248(C;T) |
| Make rs5750248(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36306846 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5750248 |
| dbSNP (classic) | rs5750248 |
| ClinGen | rs5750248 |
| ebi | rs5750248 |
| HLI | rs5750248 |
| Exac | rs5750248 |
| Gnomad | rs5750248 |
| Varsome | rs5750248 |
| LitVar | rs5750248 |
| Map | rs5750248 |
| PheGenI | rs5750248 |
| Biobank | rs5750248 |
| 1000 genomes | rs5750248 |
| hgdp | rs5750248 |
| ensembl | rs5750248 |
| geneview | rs5750248 |
| scholar | rs5750248 |
| rs5750248 | |
| pharmgkb | rs5750248 |
| gwascentral | rs5750248 |
| openSNP | rs5750248 |
| 23andMe | rs5750248 |
| SNPshot | rs5750248 |
| SNPdbe | rs5750248 |
| MSV3d | rs5750248 |
| GWAS Ctlg | rs5750248 |
| GMAF | 0.1598 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20144966
] African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
[PMID 20124285] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15
[PMID 22956460] Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.
