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rs28942098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28942098(A;A)
Make rs28942098(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position193122203
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs28942098
ebirs28942098
HLIrs28942098
Exacrs28942098
Varsomers28942098
Maprs28942098
PheGenIrs28942098
hapmaprs28942098
1000 genomesrs28942098
hgdprs28942098
ensemblrs28942098
gopubmedrs28942098
geneviewrs28942098
scholarrs28942098
googlers28942098
pharmgkbrs28942098
gwascentralrs28942098
openSNPrs28942098
23andMers28942098
23andMe allrs28942098
SNP Nexus

SNPshotrs28942098
SNPdbers28942098
MSV3drs28942098
GWAS Ctlgrs28942098
Max Magnitude0
OMIM607393
DescHYPERPARATHYROIDISM-JAW TUMOR SYNDROME
Variant0001
Relatedalso


ClinVar
Risk rs28942098(A;A)
Alt rs28942098(A;A)
Reference rs28942098(G;G)
Significance Pathogenic
Disease Hyperparathyroidism 2
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 2
Reversed 0
HGVS NC_000001.10:g.193091333G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003424.2,