CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Ceruloplasmin deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553759338
rs1553759338
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0878682
Disease:
Ceruloplasmin deficiency 		A 0.700 CausalMutation CLINVAR Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 26777753 2016