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rs587776559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776559(A;A)
Make rs587776559(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position193130173
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs587776559
ebirs587776559
HLIrs587776559
Exacrs587776559
Varsomers587776559
Maprs587776559
PheGenIrs587776559
hapmaprs587776559
1000 genomesrs587776559
hgdprs587776559
ensemblrs587776559
gopubmedrs587776559
geneviewrs587776559
scholarrs587776559
googlers587776559
pharmgkbrs587776559
gwascentralrs587776559
openSNPrs587776559
23andMers587776559
23andMe allrs587776559
SNP Nexus

SNPshotrs587776559
SNPdbers587776559
MSV3drs587776559
GWAS Ctlgrs587776559
Max Magnitude0
ClinVar
Risk rs587776559(A;A)
Alt rs587776559(A;A)
Reference rs587776559(G;G)
Significance Pathogenic
Disease Hyperparathyroidism 2
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 2
Reversed 0
HGVS NC_000001.10:g.193099303G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003440.2,