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rs5750250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs5750250(A;G)
Make rs5750250(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position36312438
GeneMYH9
is asnp
is mentioned by
dbSNPrs5750250
ebirs5750250
HLIrs5750250
Exacrs5750250
Varsomers5750250
Maprs5750250
PheGenIrs5750250
hapmaprs5750250
1000 genomesrs5750250
hgdprs5750250
ensemblrs5750250
gopubmedrs5750250
geneviewrs5750250
scholarrs5750250
googlers5750250
pharmgkbrs5750250
gwascentralrs5750250
openSNPrs5750250
23andMers5750250
23andMe allrs5750250
SNP Nexus

SNPshotrs5750250
SNPdbers5750250
MSV3drs5750250
GWAS Ctlgrs5750250
GMAF0.1529
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[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 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.