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rs6435957

From SNPedia

Orientationplus
Stabilizedplus
Make rs6435957(C;C)
Make rs6435957(C;T)
Make rs6435957(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position217013486
is asnp
is mentioned by
dbSNPrs6435957
ebirs6435957
HLIrs6435957
Exacrs6435957
Varsomers6435957
Maprs6435957
PheGenIrs6435957
hapmaprs6435957
1000 genomesrs6435957
hgdprs6435957
ensemblrs6435957
gopubmedrs6435957
geneviewrs6435957
scholarrs6435957
googlers6435957
pharmgkbrs6435957
gwascentralrs6435957
openSNPrs6435957
23andMers6435957
23andMe allrs6435957
SNP Nexus

SNPshotrs6435957
SNPdbers6435957
MSV3drs6435957
GWAS Ctlgrs6435957
GMAF0.4054
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 4E-7
Odds Ratio 0.37 [NR] % variance explained