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: rs25409
rs25409
0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy
Nervous System Diseases 0.020 1.000 2 2008 2011
dbSNP: rs4906902
rs4906902
0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy
Nervous System Diseases 0.020 < 0.001 2 2007 2012
dbSNP: rs71651682
rs71651682
0.925 0.040 15 26772759 missense variant C/T snv
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy
Nervous System Diseases 0.020 1.000 2 2008 2012