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rs13058467

From SNPedia

Orientationplus
Stabilizedplus
Make rs13058467(C;C)
Make rs13058467(C;T)
Make rs13058467(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position43183043
GeneTTLL12
is asnp
is mentioned by
dbSNPrs13058467
ebirs13058467
HLIrs13058467
Exacrs13058467
Varsomers13058467
Maprs13058467
PheGenIrs13058467
hapmaprs13058467
1000 genomesrs13058467
hgdprs13058467
ensemblrs13058467
gopubmedrs13058467
geneviewrs13058467
scholarrs13058467
googlers13058467
pharmgkbrs13058467
gwascentralrs13058467
openSNPrs13058467
23andMers13058467
23andMe allrs13058467
SNP Nexus

SNPshotrs13058467
SNPdbers13058467
MSV3drs13058467
GWAS Ctlgrs13058467
GMAF0.06061
Max Magnitude
? (C;C) (C;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 C
P-val 4E-7
Odds Ratio 4.40 [2.5-7.8]