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rs12532

From SNPedia

Orientationplus
Stabilizedplus
Make rs12532(A;A)
Make rs12532(A;G)
Make rs12532(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position4863419
GeneMSX1
is asnp
is mentioned by
dbSNPrs12532
ebirs12532
HLIrs12532
Exacrs12532
Varsomers12532
Maprs12532
PheGenIrs12532
hapmaprs12532
1000 genomesrs12532
hgdprs12532
ensemblrs12532
gopubmedrs12532
geneviewrs12532
scholarrs12532
googlers12532
pharmgkbrs12532
gwascentralrs12532
openSNPrs12532
23andMers12532
23andMe allrs12532
SNP Nexus

SNPshotrs12532
SNPdbers12532
MSV3drs12532
GWAS Ctlgrs12532
GMAF0.4298
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20635363] Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate


[PMID 20450679] [Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis: a case-control study].


[PMID 21689018] Association between MSX1 variants and oral clefts in Han Chinese in western China.


[PMID 23231047] Association Between CDH1 and MSX1 Gene Polymorphisms and the Risk of Nonsyndromic Cleft Lip and/or Cleft Palate in a Southeast Iranian Population


[PMID 23580168OA-icon.png] Association between MSX1 SNPs and Nonsyndromic Cleft Lip with or without Cleft Palate in the Korean Population


[PMID 24603642] A miRNA-binding-site SNP of MSX1 is Associated with NSOC Susceptibility


[PMID 23549991OA-icon.png] Candidate gene studies in hypodontia suggest role for FGF3.