Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121434579
rs121434579 		0.925 0.040 5 161895774 missense variant C/A snv
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.800 1.000 1 2002 2002
dbSNP: rs587777364
rs587777364 		1.000 5 161882653 missense variant G/A snv
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.800 1.000 1 2011 2011
dbSNP: rs587777308
rs587777308 		0.763 0.040 5 161873196 missense variant G/A snv
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.700 1.000 3 2014 2016
dbSNP: rs886039373
rs886039373 		0.882 0.040 5 161882639 missense variant G/A snv
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.700 1.000 1 2016 2016
dbSNP: rs1561587715
rs1561587715 		0.925 0.040 5 161895676 frameshift variant TGCTCACCATGACAACATTG/- delins
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.700 0
dbSNP: rs796052492
rs796052492 		0.925 0.040 5 161890993 missense variant C/A snv
CUI: C4013473
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 		0.700 0