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rs10740993

From SNPedia

Orientationplus
Stabilizedplus
Make rs10740993(C;C)
Make rs10740993(C;T)
Make rs10740993(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position18153553
GeneCACNB2
is asnp
is mentioned by
dbSNPrs10740993
ebirs10740993
HLIrs10740993
Exacrs10740993
Varsomers10740993
Maprs10740993
PheGenIrs10740993
hapmaprs10740993
1000 genomesrs10740993
hgdprs10740993
ensemblrs10740993
gopubmedrs10740993
geneviewrs10740993
scholarrs10740993
googlers10740993
pharmgkbrs10740993
gwascentralrs10740993
openSNPrs10740993
23andMers10740993
23andMe allrs10740993
SNP Nexus

SNPshotrs10740993
SNPdbers10740993
MSV3drs10740993
GWAS Ctlgrs10740993
GMAF0.4757
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 2E-9
Odds Ratio .14 [0.096-0.186] unit increase