CASR, calcium sensing receptor, 846

N. diseases: 517; N. variants: 131
Disease: Hypoparathyroidism - autosomal dominant ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893701
rs104893701
Entrez Id: 846
Gene Symbol: CASR
CASR
CUI: C0342345
Disease:
Hypoparathyroidism - autosomal dominant 		G 0.700 CausalMutation CLINVAR