rs3769955, SCN2A

N. diseases: 1
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 1.000 0.080 2 165378122 intron variant C/T snv 0.42 0.700 1.000 1 2014 2014