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rs3821949

From SNPedia

Orientationplus
Stabilizedplus
Make rs3821949(A;A)
Make rs3821949(A;G)
Make rs3821949(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position4858675
GeneMSX1
is asnp
is mentioned by
dbSNPrs3821949
ebirs3821949
HLIrs3821949
Exacrs3821949
Varsomers3821949
Maprs3821949
PheGenIrs3821949
hapmaprs3821949
1000 genomesrs3821949
hgdprs3821949
ensemblrs3821949
gopubmedrs3821949
geneviewrs3821949
scholarrs3821949
googlers3821949
pharmgkbrs3821949
gwascentralrs3821949
openSNPrs3821949
23andMers3821949
23andMe allrs3821949
SNP Nexus

SNPshotrs3821949
SNPdbers3821949
MSV3drs3821949
GWAS Ctlgrs3821949
GMAF0.3499
Max Magnitude
? (A;A) (A;G) (G;G) 28
[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 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.