rs211037, GABRG2

N. diseases: 14
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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.060 0.667 6 2010 2018
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.050 0.800 5 2012 2018
Seizures
CUI: C0036572
Disease: Seizures
553 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.040 0.750 4 2010 2018
Juvenile Myoclonic Epilepsy
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
46 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.030 0.667 3 2013 2018
Idiopathic generalized epilepsy
CUI: C0270850
Disease: Idiopathic generalized epilepsy
24 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.020 1.000 2 2013 2018
Absence Epilepsy
CUI: C0014553
Disease: Absence Epilepsy
17 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2002 2002
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2015 2015
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2018 2018
Hepatic Encephalopathy
CUI: C0019151
Disease: Hepatic Encephalopathy
3 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2014 2014
Hypoalbuminemia
CUI: C0239981
Disease: Hypoalbuminemia
9 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2014 2014
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2012 2012
Recurrent seizure
CUI: C0748607
Disease: Recurrent seizure
1 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2018 2018
Seizures, Focal
CUI: C0751495
Disease: Seizures, Focal
15 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2016 2016
Symptomatic epilepsy
CUI: C1406659
Disease: Symptomatic epilepsy
9 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2016 2016