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rs5750248

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs5750248(C;T)
Make rs5750248(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36306846
GeneMYH9
is asnp
is mentioned by
dbSNPrs5750248
ebirs5750248
HLIrs5750248
Exacrs5750248
Varsomers5750248
Maprs5750248
PheGenIrs5750248
hapmaprs5750248
1000 genomesrs5750248
hgdprs5750248
ensemblrs5750248
gopubmedrs5750248
geneviewrs5750248
scholarrs5750248
googlers5750248
pharmgkbrs5750248
gwascentralrs5750248
openSNPrs5750248
23andMers5750248
23andMe allrs5750248
SNP Nexus

SNPshotrs5750248
SNPdbers5750248
MSV3drs5750248
GWAS Ctlgrs5750248
GMAF0.1598
Max Magnitude0
? (C;C) (C;T) (T;T) 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 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.