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rs4821481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4821481(C;C)
Make rs4821481(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36299896
GeneMYH9
is asnp
is mentioned by
dbSNPrs4821481
ebirs4821481
HLIrs4821481
Exacrs4821481
Varsomers4821481
Maprs4821481
PheGenIrs4821481
hapmaprs4821481
1000 genomesrs4821481
hgdprs4821481
ensemblrs4821481
gopubmedrs4821481
geneviewrs4821481
scholarrs4821481
googlers4821481
pharmgkbrs4821481
gwascentralrs4821481
openSNPrs4821481
23andMers4821481
23andMe allrs4821481
SNP Nexus

SNPshotrs4821481
SNPdbers4821481
MSV3drs4821481
GWAS Ctlgrs4821481
GMAF0.1795
Max Magnitude0
? (C;C) (C;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 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 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 22956460OA-icon.png] Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.