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rs3752462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3752462(C;C)
Make rs3752462(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36314138
GeneMYH9
is asnp
is mentioned by
dbSNPrs3752462
ebirs3752462
HLIrs3752462
Exacrs3752462
Varsomers3752462
Maprs3752462
PheGenIrs3752462
hapmaprs3752462
1000 genomesrs3752462
hgdprs3752462
ensemblrs3752462
gopubmedrs3752462
geneviewrs3752462
scholarrs3752462
googlers3752462
pharmgkbrs3752462
gwascentralrs3752462
openSNPrs3752462
23andMers3752462
23andMe allrs3752462
SNP Nexus

SNPshotrs3752462
SNPdbers3752462
MSV3drs3752462
GWAS Ctlgrs3752462
GMAF0.4532
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19153477OA-icon.png] 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

OMIM119530
Desc
Variant
Relatedalso
[PMID 21968013OA-icon.png] Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans


[PMID 18716610OA-icon.png] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.


[PMID 18794854OA-icon.png] MYH9 is associated with nondiabetic end-stage renal disease in African Americans.


[PMID 18794856OA-icon.png] MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.


[PMID 19177153OA-icon.png] 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 19764949OA-icon.png] Potential donor-recipient MYH9 genotype interactions in posttransplant nephrotic syndrome after pediatric kidney transplantation.


[PMID 20124285OA-icon.png] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.


[PMID 20144966OA-icon.png] African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.


[PMID 20634883OA-icon.png] 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 22956460OA-icon.png] 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
Variation info
Gene MYH9
CLNDBN not specified
Reversed 0
HGVS NC_000022.10:g.36710183T>C
CLNSRC ClinVar
CLNACC RCV000037547.2,