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

rs121434265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434265(C;G)
Make rs121434265(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position193125142
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs121434265
ebirs121434265
HLIrs121434265
Exacrs121434265
Varsomers121434265
Maprs121434265
PheGenIrs121434265
hapmaprs121434265
1000 genomesrs121434265
hgdprs121434265
ensemblrs121434265
gopubmedrs121434265
geneviewrs121434265
scholarrs121434265
googlers121434265
pharmgkbrs121434265
gwascentralrs121434265
openSNPrs121434265
23andMers121434265
23andMe allrs121434265
SNP Nexus

SNPshotrs121434265
SNPdbers121434265
MSV3drs121434265
GWAS Ctlgrs121434265
Max Magnitude0
OMIM607393
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121434265(G;G)
Alt rs121434265(G;G)
Reference rs121434265(C;C)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193094272C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003433.4,