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rs11089788

From SNPedia

Orientationplus
Stabilizedplus
Make rs11089788(A;A)
Make rs11089788(A;C)
Make rs11089788(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position36355056
GeneMYH9
is asnp
is mentioned by
dbSNPrs11089788
ebirs11089788
HLIrs11089788
Exacrs11089788
Varsomers11089788
Maprs11089788
PheGenIrs11089788
hapmaprs11089788
1000 genomesrs11089788
hgdprs11089788
ensemblrs11089788
gopubmedrs11089788
geneviewrs11089788
scholarrs11089788
googlers11089788
pharmgkbrs11089788
gwascentralrs11089788
openSNPrs11089788
23andMers11089788
23andMe allrs11089788
SNP Nexus

SNPshotrs11089788
SNPdbers11089788
MSV3drs11089788
GWAS Ctlgrs11089788
GMAF0.3549
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 19387472] Genome-wide linkage analysis of serum creatinine in three isolated European populations


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


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


[PMID 23516419OA-icon.png] Epistatic Role of the MYH9/APOL1 Region on Familial Hematuria Genes