rs12532

Orientation

plus

Stabilized

plus

Make rs12532(A;A)

Make rs12532(A;G)

Make rs12532(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4863419

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs12532
dbSNP (classic)	rs12532
ClinGen	rs12532
ebi	rs12532
HLI	rs12532
Exac	rs12532
Gnomad	rs12532
Varsome	rs12532
LitVar	rs12532
Map	rs12532
PheGenI	rs12532
Biobank	rs12532
1000 genomes	rs12532
hgdp	rs12532
ensembl	rs12532
geneview	rs12532
scholar	rs12532
google	rs12532
pharmgkb	rs12532
gwascentral	rs12532
openSNP	rs12532
23andMe	rs12532
SNPshot	rs12532
SNPdbe	rs12532
MSV3d	rs12532
GWAS Ctlg	rs12532

GMAF

0.4298

Max Magnitude

0

?	(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 23580168] 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 23549991] Candidate gene studies in hypodontia suggest role for FGF3.

[PMID 31781599] Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.