Have questions? Visit https://www.reddit.com/r/SNPedia

rs4821480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4821480(G;G)
Make rs4821480(G;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36299201
GeneMYH9
is asnp
is mentioned by
dbSNPrs4821480
ebirs4821480
HLIrs4821480
Exacrs4821480
Varsomers4821480
Maprs4821480
PheGenIrs4821480
hapmaprs4821480
1000 genomesrs4821480
hgdprs4821480
ensemblrs4821480
gopubmedrs4821480
geneviewrs4821480
scholarrs4821480
googlers4821480
pharmgkbrs4821480
gwascentralrs4821480
openSNPrs4821480
23andMers4821480
23andMe allrs4821480
SNP Nexus

SNPshotrs4821480
SNPdbers4821480
MSV3drs4821480
GWAS Ctlgrs4821480
GMAF0.1795
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19567477OA-icon.png] Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD
OMIM612551
DescFOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO; FSGS4
Variant
Relatedalso
[PMID 20124285OA-icon.png] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15

[PMID 21245129] Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese


[PMID 21429915OA-icon.png] The MYH9/APOL1 region and Chronic Kidney Disease in European-Americans


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


[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 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 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 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.