rs2032487
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2032487(C;C) |
| Make rs2032487(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36299382 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2032487 |
| dbSNP (classic) | rs2032487 |
| ClinGen | rs2032487 |
| ebi | rs2032487 |
| HLI | rs2032487 |
| Exac | rs2032487 |
| Gnomad | rs2032487 |
| Varsome | rs2032487 |
| LitVar | rs2032487 |
| Map | rs2032487 |
| PheGenI | rs2032487 |
| Biobank | rs2032487 |
| 1000 genomes | rs2032487 |
| hgdp | rs2032487 |
| ensembl | rs2032487 |
| geneview | rs2032487 |
| scholar | rs2032487 |
| rs2032487 | |
| pharmgkb | rs2032487 |
| gwascentral | rs2032487 |
| openSNP | rs2032487 |
| 23andMe | rs2032487 |
| SNPshot | rs2032487 |
| SNPdbe | rs2032487 |
| MSV3d | rs2032487 |
| GWAS Ctlg | rs2032487 |
| GMAF | 0.1809 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19567477
] Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD
[PMID 19153477] Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study
[PMID 21968013] Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
[PMID 18794854] MYH9 is associated with nondiabetic end-stage renal disease in African Americans.
[PMID 18794856] MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
[PMID 19177153] Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.
[PMID 19764949] Potential donor-recipient MYH9 genotype interactions in posttransplant nephrotic syndrome after pediatric kidney transplantation.
[PMID 20124285] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
[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 20634883] Worldwide distribution of the MYH9 kidney disease susceptibility alleles and haplotypes: evidence of historical selection in Africa.
[PMID 22956460] Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.
