rs730882211, SEC24D

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 1.000 0.040 4 118815132 missense variant C/G snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 1.000 0.040 4 118815132 missense variant C/G snv 0.700 0