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rs739097

From SNPedia

Orientationplus
Stabilizedplus
Make rs739097(A;A)
Make rs739097(A;G)
Make rs739097(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position36350034
GeneMYH9
is asnp
is mentioned by
dbSNPrs739097
ebirs739097
HLIrs739097
Exacrs739097
Varsomers739097
Maprs739097
PheGenIrs739097
hapmaprs739097
1000 genomesrs739097
hgdprs739097
ensemblrs739097
gopubmedrs739097
geneviewrs739097
scholarrs739097
googlers739097
pharmgkbrs739097
gwascentralrs739097
openSNPrs739097
23andMers739097
23andMe allrs739097
SNP Nexus

SNPshotrs739097
SNPdbers739097
MSV3drs739097
GWAS Ctlgrs739097
GMAF0.4949
Max Magnitude
? (A;A) (A;G) (G;G) 28

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

[PMID 18571626] RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.

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