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.
Early Infantile Epileptic Encephalopathy 6
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
392 0.851 0.040 2 166009745 missense variant C/G snv 0.700 1.000 21 2003 2017
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.851 0.040 2 166009745 missense variant C/G snv 0.010 1.000 1 2017 2017
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
43 0.851 0.040 2 166009745 missense variant C/G snv 0.010 1.000 1 2017 2017
Infantile Severe Myoclonic Epilepsy
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
32 0.851 0.040 2 166009745 missense variant C/G snv 0.010 1.000 1 2017 2017