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rs121434601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434601(C;T)
Make rs121434601(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46898097
GenePTH1R
is asnp
is mentioned by
dbSNPrs121434601
ebirs121434601
HLIrs121434601
Exacrs121434601
Varsomers121434601
Maprs121434601
PheGenIrs121434601
hapmaprs121434601
1000 genomesrs121434601
hgdprs121434601
ensemblrs121434601
gopubmedrs121434601
geneviewrs121434601
scholarrs121434601
googlers121434601
pharmgkbrs121434601
gwascentralrs121434601
openSNPrs121434601
23andMers121434601
23andMe allrs121434601
SNP Nexus

SNPshotrs121434601
SNPdbers121434601
MSV3drs121434601
GWAS Ctlgrs121434601
Max Magnitude0
ClinVar
Risk rs121434601(T;T)
Alt rs121434601(T;T)
Reference rs121434601(C;C)
Significance Untested
Disease
Variation info
Gene PTH1R
CLNDBN
Reversed 0
HGVS NC_000003.11:g.46939587C>T
CLNSRC
CLNACC