rs694539, NNMT

N. diseases: 10
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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.020 1.000 2 2012 2014
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2013 2013
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2016 2016
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2016 2016
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2013 2013
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2012 2012
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1 2016 2016
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2016 2016
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.776 0.200 11 114262697 intron variant C/T snv 0.21 0.010 1.000 1 2013 2013