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rs2413396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(T;T) 0 common in complete genomics
Make rs2413396(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36312039
GeneMYH9
is asnp
is mentioned by
dbSNPrs2413396
ebirs2413396
HLIrs2413396
Exacrs2413396
Varsomers2413396
Maprs2413396
PheGenIrs2413396
hapmaprs2413396
1000 genomesrs2413396
hgdprs2413396
ensemblrs2413396
gopubmedrs2413396
geneviewrs2413396
scholarrs2413396
googlers2413396
pharmgkbrs2413396
gwascentralrs2413396
openSNPrs2413396
23andMers2413396
23andMe allrs2413396
SNP Nexus

SNPshotrs2413396
SNPdbers2413396
MSV3drs2413396
GWAS Ctlgrs2413396
GMAF0.1947
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20124285OA-icon.png] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15


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


[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.


ClinVar
Risk rs2413396(T;T)
Alt rs2413396(T;T)
Reference rs2413396(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MYH9
CLNDBN not specified
Reversed 0
HGVS NC_000022.10:g.36708084C>T
CLNSRC ClinVar
CLNACC RCV000037548.2,