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rs5995288

From SNPedia

Orientationplus
Stabilizedplus
Make rs5995288(C;C)
Make rs5995288(C;T)
Make rs5995288(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36366589
GeneMYH9
is asnp
is mentioned by
dbSNPrs5995288
ebirs5995288
HLIrs5995288
Exacrs5995288
Varsomers5995288
Maprs5995288
PheGenIrs5995288
hapmaprs5995288
1000 genomesrs5995288
hgdprs5995288
ensemblrs5995288
gopubmedrs5995288
geneviewrs5995288
scholarrs5995288
googlers5995288
pharmgkbrs5995288
gwascentralrs5995288
openSNPrs5995288
23andMers5995288
23andMe allrs5995288
SNP Nexus

SNPshotrs5995288
SNPdbers5995288
MSV3drs5995288
GWAS Ctlgrs5995288
GMAF0.4784
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.