Have questions? Visit https://www.reddit.com/r/SNPedia

rs121434263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434263(A;A)
Make rs121434263(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position193122328
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs121434263
ebirs121434263
HLIrs121434263
Exacrs121434263
Varsomers121434263
Maprs121434263
PheGenIrs121434263
hapmaprs121434263
1000 genomesrs121434263
hgdprs121434263
ensemblrs121434263
gopubmedrs121434263
geneviewrs121434263
scholarrs121434263
googlers121434263
pharmgkbrs121434263
gwascentralrs121434263
openSNPrs121434263
23andMers121434263
23andMe allrs121434263
SNP Nexus

SNPshotrs121434263
SNPdbers121434263
MSV3drs121434263
GWAS Ctlgrs121434263
Max Magnitude0
OMIM607393
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121434263(A;A)
Alt rs121434263(A;A)
Reference rs121434263(G;G)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193091458G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003430.4,