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rs794727303

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727303(G;T)
Make rs794727303(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position193125218
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs794727303
ebirs794727303
HLIrs794727303
Exacrs794727303
Varsomers794727303
Maprs794727303
PheGenIrs794727303
hapmaprs794727303
1000 genomesrs794727303
hgdprs794727303
ensemblrs794727303
gopubmedrs794727303
geneviewrs794727303
scholarrs794727303
googlers794727303
pharmgkbrs794727303
gwascentralrs794727303
openSNPrs794727303
23andMers794727303
23andMe allrs794727303
SNP Nexus

SNPshotrs794727303
SNPdbers794727303
MSV3drs794727303
GWAS Ctlgrs794727303
Max Magnitude0
ClinVar
Risk rs794727303(T;T)
Alt rs794727303(T;T)
Reference rs794727303(G;G)
Significance Pathogenic
Disease Hyperparathyroidism 1 Hyperparathyroidism 2
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 1 Hyperparathyroidism 2
Reversed 0
HGVS NC_000001.10:g.193094348G>T
CLNSRC
CLNACC RCV000175944.1, RCV000175945.1,