rs2304016, 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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 2 165311993 intron variant A/G snv 1.2E-02 4.8E-03 0.010 1 2019 2019
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 0.925 0.040 2 165311993 intron variant A/G snv 1.2E-02 4.8E-03 0.010 1.000 1 2019 2019