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rs121434262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434262(C;T)
Make rs121434262(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position193122225
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs121434262
ebirs121434262
HLIrs121434262
Exacrs121434262
Varsomers121434262
Maprs121434262
PheGenIrs121434262
hapmaprs121434262
1000 genomesrs121434262
hgdprs121434262
ensemblrs121434262
gopubmedrs121434262
geneviewrs121434262
scholarrs121434262
googlers121434262
pharmgkbrs121434262
gwascentralrs121434262
openSNPrs121434262
23andMers121434262
23andMe allrs121434262
SNP Nexus

SNPshotrs121434262
SNPdbers121434262
MSV3drs121434262
GWAS Ctlgrs121434262
Max Magnitude0
OMIM607393
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434262(T;T)
Alt rs121434262(T;T)
Reference rs121434262(C;C)
Significance Pathogenic
Disease Hyperparathyroidism 2
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 2
Reversed 0
HGVS NC_000001.10:g.193091355C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003425.2,