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rs587776558

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776558(A;A)
Make rs587776558(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position193122332
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs587776558
ebirs587776558
HLIrs587776558
Exacrs587776558
Varsomers587776558
Maprs587776558
PheGenIrs587776558
hapmaprs587776558
1000 genomesrs587776558
hgdprs587776558
ensemblrs587776558
gopubmedrs587776558
geneviewrs587776558
scholarrs587776558
googlers587776558
pharmgkbrs587776558
gwascentralrs587776558
openSNPrs587776558
23andMers587776558
23andMe allrs587776558
SNP Nexus

SNPshotrs587776558
SNPdbers587776558
MSV3drs587776558
GWAS Ctlgrs587776558
Max Magnitude0
ClinVar
Risk rs587776558(A;A)
Alt rs587776558(A;A)
Reference rs587776558(G;G)
Significance Pathogenic
Disease Hyperparathyroidism 1 Parathyroid adenoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 1 Parathyroid adenoma, somatic
Reversed 0
HGVS NC_000001.10:g.193091462G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003435.2, RCV000003436.4,