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rs587776557

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776557(-;-)
Make rs587776557(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position193122253
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs587776557
ebirs587776557
HLIrs587776557
Exacrs587776557
Varsomers587776557
Maprs587776557
PheGenIrs587776557
hapmaprs587776557
1000 genomesrs587776557
hgdprs587776557
ensemblrs587776557
gopubmedrs587776557
geneviewrs587776557
scholarrs587776557
googlers587776557
pharmgkbrs587776557
gwascentralrs587776557
openSNPrs587776557
23andMers587776557
23andMe allrs587776557
SNP Nexus

SNPshotrs587776557
SNPdbers587776557
MSV3drs587776557
GWAS Ctlgrs587776557
Max Magnitude0
ClinVar
Risk rs587776557(;)
Alt rs587776557(;)
Reference rs587776557(T;T)
Significance Pathogenic
Disease Cystic parathyroid adenoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Cystic parathyroid adenoma
Reversed 0
HGVS NC_000001.10:g.193091383delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003432.4,