rs3752462
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs3752462(C;C) |
| Make rs3752462(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36314138 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3752462 |
| dbSNP (classic) | rs3752462 |
| ClinGen | rs3752462 |
| ebi | rs3752462 |
| HLI | rs3752462 |
| Exac | rs3752462 |
| Gnomad | rs3752462 |
| Varsome | rs3752462 |
| LitVar | rs3752462 |
| Map | rs3752462 |
| PheGenI | rs3752462 |
| Biobank | rs3752462 |
| 1000 genomes | rs3752462 |
| hgdp | rs3752462 |
| ensembl | rs3752462 |
| geneview | rs3752462 |
| scholar | rs3752462 |
| rs3752462 | |
| pharmgkb | rs3752462 |
| gwascentral | rs3752462 |
| openSNP | rs3752462 |
| 23andMe | rs3752462 |
| SNPshot | rs3752462 |
| SNPdbe | rs3752462 |
| MSV3d | rs3752462 |
| GWAS Ctlg | rs3752462 |
| GMAF | 0.4532 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19153477
] Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study
[PMID 19891592] Association Among Polymorphisms at MYH9, Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China
[PMID 21245129] Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese
[PMID 21968013] Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
[PMID 18716610] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
[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 23470845] Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort
[PMID 22956460] Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.
| ClinVar | |
|---|---|
| Risk | rs3752462(C;C) |
| Alt | rs3752462(C;C) |
| Reference | Rs3752462(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified Nonsyndromic Hearing Loss MYH9-related disorder |
| Variation | info |
| Gene | MYH9 |
| CLNDBN | not specified Nonsyndromic Hearing Loss, Dominant MYH9-related disorder |
| Reversed | 0 |
| HGVS | NC_000022.10:g.36710183T>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000037547.3, RCV000334868.1, RCV000392730.1, |
[PMID 29862302] Association between MYH9 and APOL1 Gene Polymorphisms and the Risk of Diabetic Kidney Disease in Patients with Type 2 Diabetes in a Chinese Han Population.
[PMID 32873246] Effect of donor non-muscle myosin heavy chain (MYH9) gene polymorphisms on clinically relevant kidney allograft dysfunction.
