rs2904551, PRODH

N. diseases: 8
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 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.810 1.000 4 2002 2018
SCHIZOPHRENIA 4 (disorder)
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
7 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.700 1.000 2 2002 2005
Hyperprolinemia
CUI: C0268528
Disease: Hyperprolinemia
3 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.020 1.000 2 2002 2005
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.010 1.000 1 2018 2018
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.010 1.000 1 2018 2018
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.010 1.000 1 2018 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.010 1.000 1 2018 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 0.010 1.000 1 2018 2018