rs386134141, CP

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ceruloplasmin deficiency
CUI: C0878682
Disease: Ceruloplasmin deficiency
0.700 GeneticVariation CLINVAR
Ceruloplasmin deficiency
CUI: C0878682
Disease: Ceruloplasmin deficiency
0.700 CausalMutation CLINVAR
Iron-Refractory Iron Deficiency Anemia
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
0.700 GeneticVariation CLINVAR
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.700 GeneticVariation CLINVAR