rs11912763
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs11912763(A;A) |
| Make rs11912763(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36288676 |
| Gene | MIR6819, MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11912763 |
| dbSNP (classic) | rs11912763 |
| ClinGen | rs11912763 |
| ebi | rs11912763 |
| HLI | rs11912763 |
| Exac | rs11912763 |
| Gnomad | rs11912763 |
| Varsome | rs11912763 |
| LitVar | rs11912763 |
| Map | rs11912763 |
| PheGenI | rs11912763 |
| Biobank | rs11912763 |
| 1000 genomes | rs11912763 |
| hgdp | rs11912763 |
| ensembl | rs11912763 |
| geneview | rs11912763 |
| scholar | rs11912763 |
| rs11912763 | |
| pharmgkb | rs11912763 |
| gwascentral | rs11912763 |
| openSNP | rs11912763 |
| 23andMe | rs11912763 |
| SNPshot | rs11912763 |
| SNPdbe | rs11912763 |
| MSV3d | rs11912763 |
| GWAS Ctlg | rs11912763 |
| GMAF | 0.04132 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 20635188] Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene
[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.
