rs211014, GABRG2

N. diseases: 2
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.
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.925 0.080 5 162149412 3 prime UTR variant C/A snv 0.30 0.010 1.000 1 2007 2007
Symptomatic epilepsy
CUI: C1406659
Disease: Symptomatic epilepsy
9 0.925 0.080 5 162149412 3 prime UTR variant C/A snv 0.30 0.010 1.000 1 2016 2016