rs3755724, TIMP4;SYN2

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.
Epilepsies, Partial
CUI: C0014547
Disease: Epilepsies, Partial
23 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2014 2014
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2009 2009
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2013 2013
Seizures
CUI: C0036572
Disease: Seizures
553 0.790 0.360 3 12159406 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015