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rs13288553

From SNPedia

Orientationplus
Stabilizedplus
Make rs13288553(G;G)
Make rs13288553(G;T)
Make rs13288553(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position84126546
is asnp
is mentioned by
dbSNPrs13288553
dbSNP (classic)rs13288553
ClinGenrs13288553
ebirs13288553
HLIrs13288553
Exacrs13288553
Gnomadrs13288553
Varsomers13288553
LitVarrs13288553
Maprs13288553
PheGenIrs13288553
Biobankrs13288553
1000 genomesrs13288553
hgdprs13288553
ensemblrs13288553
geneviewrs13288553
scholarrs13288553
googlers13288553
pharmgkbrs13288553
gwascentralrs13288553
openSNPrs13288553
23andMers13288553
SNPshotrs13288553
SNPdbers13288553
MSV3drs13288553
GWAS Ctlgrs13288553
GMAF0.08907
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 23918034]
Trait Molar-incisor hypomineralization
Title Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).
Risk Allele T
P-val 2E-6
Odds Ratio 4.25 [2.33-7.75]