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rs121434605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434605(G;T)
Make rs121434605(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46898112
GenePTH1R
is asnp
is mentioned by
dbSNPrs121434605
ebirs121434605
HLIrs121434605
Exacrs121434605
Varsomers121434605
Maprs121434605
PheGenIrs121434605
hapmaprs121434605
1000 genomesrs121434605
hgdprs121434605
ensemblrs121434605
gopubmedrs121434605
geneviewrs121434605
scholarrs121434605
googlers121434605
pharmgkbrs121434605
gwascentralrs121434605
openSNPrs121434605
23andMers121434605
23andMe allrs121434605
SNP Nexus

SNPshotrs121434605
SNPdbers121434605
MSV3drs121434605
GWAS Ctlgrs121434605
Max Magnitude0
OMIM168468
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121434605(A,T;A,T)
Alt rs121434605(A,T;A,T)
Reference rs121434605(G;G)
Significance Pathogenic
Disease Failure of tooth eruption
Variation info
Gene PTH1R
CLNDBN Failure of tooth eruption, primary
Reversed 0
HGVS NC_000003.11:g.46939602G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014761.25,