rs373363000, GABRA6

N. diseases: 3
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.
Absence Epilepsy
CUI: C0014553
Disease: Absence Epilepsy
17 0.882 0.080 5 161686327 missense variant C/A;T snv 4.0E-06; 3.3E-04 0.010 1.000 1 2011 2011
Childhood Absence Epilepsy
CUI: C4281785
Disease: Childhood Absence Epilepsy
13 0.882 0.080 5 161686327 missense variant C/A;T snv 4.0E-06; 3.3E-04 0.010 1.000 1 2011 2011
Generalized seizures
CUI: C0234533
Disease: Generalized seizures
13 0.882 0.080 5 161686327 missense variant C/A;T snv 4.0E-06; 3.3E-04 0.010 1.000 1 2011 2011