rs16850331, SCN2A

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 2 165292743 intron variant C/T snv 0.23 0.010 1.000 1 2010 2010
Idiopathic generalized epilepsy
CUI: C0270850
Disease: Idiopathic generalized epilepsy
24 0.925 0.080 2 165292743 intron variant C/T snv 0.23 0.010 1.000 1 2010 2010