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

rs587776560

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776560(-;-)
Make rs587776560(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position193122285
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs587776560
ebirs587776560
HLIrs587776560
Exacrs587776560
Varsomers587776560
Maprs587776560
PheGenIrs587776560
hapmaprs587776560
1000 genomesrs587776560
hgdprs587776560
ensemblrs587776560
gopubmedrs587776560
geneviewrs587776560
scholarrs587776560
googlers587776560
pharmgkbrs587776560
gwascentralrs587776560
openSNPrs587776560
23andMers587776560
23andMe allrs587776560
SNP Nexus

SNPshotrs587776560
SNPdbers587776560
MSV3drs587776560
GWAS Ctlgrs587776560
Max Magnitude0
ClinVar
Risk rs587776560(;)
Alt rs587776560(;)
Reference rs587776560(G;G)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193091415delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003441.4,