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rs4491709

From SNPedia

Orientationplus
Stabilizedplus
Make rs4491709(C;C)
Make rs4491709(C;T)
Make rs4491709(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position217030033
is asnp
is mentioned by
dbSNPrs4491709
ebirs4491709
HLIrs4491709
Exacrs4491709
Varsomers4491709
Maprs4491709
PheGenIrs4491709
hapmaprs4491709
1000 genomesrs4491709
hgdprs4491709
ensemblrs4491709
gopubmedrs4491709
geneviewrs4491709
scholarrs4491709
googlers4491709
pharmgkbrs4491709
gwascentralrs4491709
openSNPrs4491709
23andMers4491709
23andMe allrs4491709
SNP Nexus

SNPshotrs4491709
SNPdbers4491709
MSV3drs4491709
GWAS Ctlgrs4491709
GMAF0.4656
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21931568OA-icon.png]
Trait
Title Genome-wide association study identifies four loci associated with eruption of permanent teeth.
Risk Allele T
P-val 2E-14
Odds Ratio 0.1020 [0.07-0.13] unit decrease

Tooth Development