rs2870984, PRODH

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.700 CausalMutation CLINVAR
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.700 SusceptibilityMutation CLINVAR
SCHIZOPHRENIA 4 (disorder)
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
0.700 GeneticVariation UNIPROT
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.700 GeneticVariation CLINVAR