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rs1402366

From SNPedia

Orientationplus
Stabilizedplus
Make rs1402366(G;G)
Make rs1402366(G;T)
Make rs1402366(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position22724978
is asnp
is mentioned by
dbSNPrs1402366
ebirs1402366
HLIrs1402366
Exacrs1402366
Varsomers1402366
Maprs1402366
PheGenIrs1402366
hapmaprs1402366
1000 genomesrs1402366
hgdprs1402366
ensemblrs1402366
gopubmedrs1402366
geneviewrs1402366
scholarrs1402366
googlers1402366
pharmgkbrs1402366
gwascentralrs1402366
openSNPrs1402366
23andMers1402366
23andMe allrs1402366
SNP Nexus

SNPshotrs1402366
SNPdbers1402366
MSV3drs1402366
GWAS Ctlgrs1402366
GMAF0.1042
Max Magnitude
? (G;G) (G;T) (T;T) 28
OMIM125350
DescFAILURE OF TOOTH ERUPTION, PRIMARY; PFE
Variant
Relatedalso
[PMID 19061984OA-icon.png] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.