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rs11912763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11912763(A;A)
Make rs11912763(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position36288676
GeneMIR6819, MYH9
is asnp
is mentioned by
dbSNPrs11912763
ebirs11912763
HLIrs11912763
Exacrs11912763
Varsomers11912763
Maprs11912763
PheGenIrs11912763
hapmaprs11912763
1000 genomesrs11912763
hgdprs11912763
ensemblrs11912763
gopubmedrs11912763
geneviewrs11912763
scholarrs11912763
googlers11912763
pharmgkbrs11912763
gwascentralrs11912763
openSNPrs11912763
23andMers11912763
23andMe allrs11912763
SNP Nexus

SNPshotrs11912763
SNPdbers11912763
MSV3drs11912763
GWAS Ctlgrs11912763
GMAF0.04132
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[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 20635188OA-icon.png] Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

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


[PMID 22956460OA-icon.png] Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.