rs757609394, DEPDC5

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.
EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1
CUI: C4551983
Disease: EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1
67 1.000 0.040 22 31857483 missense variant A/G snv 3.3E-05 0.700 0