rs450046, PRODH;DGCR6

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
11 0.851 0.280 22 18913491 missense variant C/T snv 0.93 2.8E-03 0.700 0
SCHIZOPHRENIA 4 (disorder)
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
7 0.851 0.280 22 18913491 missense variant C/T snv 0.93 2.8E-03 0.700 0
22q11 Deletion Syndrome
CUI: C2936346
Disease: 22q11 Deletion Syndrome
2 0.851 0.280 22 18913491 missense variant C/T snv 0.93 2.8E-03 0.010 1.000 1 2015 2015
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.851 0.280 22 18913491 missense variant C/T snv 0.93 2.8E-03 0.010 1 2018 2018