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rs4844096

From SNPedia

Orientationplus
Stabilizedplus
Make rs4844096(A;A)
Make rs4844096(A;G)
Make rs4844096(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69585474
is asnp
is mentioned by
dbSNPrs4844096
dbSNP (classic)rs4844096
ClinGenrs4844096
ebirs4844096
HLIrs4844096
Exacrs4844096
Gnomadrs4844096
Varsomers4844096
LitVarrs4844096
Maprs4844096
PheGenIrs4844096
Biobankrs4844096
1000 genomesrs4844096
hgdprs4844096
ensemblrs4844096
geneviewrs4844096
scholarrs4844096
googlers4844096
pharmgkbrs4844096
gwascentralrs4844096
openSNPrs4844096
23andMers4844096
SNPshotrs4844096
SNPdbers4844096
MSV3drs4844096
GWAS Ctlgrs4844096
GMAF0.2267
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20195514OA-icon.png]
Trait Primary tooth development (number of teeth)
Title Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy
Risk Allele G
P-val 5E-11
Odds Ratio 0.73 [NR] % variance explained