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

rs2032487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2032487(C;C)
Make rs2032487(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36299382
GeneMYH9
is asnp
is mentioned by
dbSNPrs2032487
ebirs2032487
HLIrs2032487
Exacrs2032487
Varsomers2032487
Maprs2032487
PheGenIrs2032487
hapmaprs2032487
1000 genomesrs2032487
hgdprs2032487
ensemblrs2032487
gopubmedrs2032487
geneviewrs2032487
scholarrs2032487
googlers2032487
pharmgkbrs2032487
gwascentralrs2032487
openSNPrs2032487
23andMers2032487
23andMe allrs2032487
SNP Nexus

SNPshotrs2032487
SNPdbers2032487
MSV3drs2032487
GWAS Ctlgrs2032487
GMAF0.1809
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 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 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.