rs2904552, PRODH

N. diseases: 3
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
0.800 GeneticVariation UNIPROT Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. 17135275 2007
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 GeneticVariation UNIPROT Functional consequences of PRODH missense mutations. 15662599 2005
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 GeneticVariation UNIPROT PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. 12217952 2002
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 SusceptibilityMutation CLINVAR
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 CausalMutation CLINVAR
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.010 GeneticVariation BEFREE One polymorphism was associated with schizophrenia (rs2904552), with the G-allele more frequent in patients than in controls. 24498354 2014