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rs7078

From SNPedia

Orientationminus
Stabilizedminus
Make rs7078(C;C)
Make rs7078(C;T)
Make rs7078(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36281868
GeneMYH9
is asnp
is mentioned by
dbSNPrs7078
ebirs7078
HLIrs7078
Exacrs7078
Varsomers7078
Maprs7078
PheGenIrs7078
hapmaprs7078
1000 genomesrs7078
hgdprs7078
ensemblrs7078
gopubmedrs7078
geneviewrs7078
scholarrs7078
googlers7078
pharmgkbrs7078
gwascentralrs7078
openSNPrs7078
23andMers7078
23andMe allrs7078
SNP Nexus

SNPshotrs7078
SNPdbers7078
MSV3drs7078
GWAS Ctlgrs7078
GMAF0.2011
Max Magnitude

[PMID 19320731] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate


[PMID 18716610OA-icon.png] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.


[PMID 18794854OA-icon.png] MYH9 is associated with nondiabetic end-stage renal disease in African Americans.


[PMID 18794856OA-icon.png] MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.


[PMID 19177153OA-icon.png] Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.


[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.