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rs11796357

From SNPedia

Orientationplus
Stabilizedplus
Make rs11796357(A;A)
Make rs11796357(A;G)
Make rs11796357(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69578860
is asnp
is mentioned by
dbSNPrs11796357
ebirs11796357
HLIrs11796357
Exacrs11796357
Varsomers11796357
Maprs11796357
PheGenIrs11796357
hapmaprs11796357
1000 genomesrs11796357
hgdprs11796357
ensemblrs11796357
gopubmedrs11796357
geneviewrs11796357
scholarrs11796357
googlers11796357
pharmgkbrs11796357
gwascentralrs11796357
openSNPrs11796357
23andMers11796357
23andMe allrs11796357
SNP Nexus

SNPshotrs11796357
SNPdbers11796357
MSV3drs11796357
GWAS Ctlgrs11796357
GMAF0.1131
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23704328OA-icon.png]
Trait Primary tooth development (number of teeth)
Title Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
Risk Allele G
P-val 7E-19
Odds Ratio .20 [0.16-0.24] unit increase