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: rs2351299
rs2351299
1.000 0.040 4 47141348 intron variant G/T snv 0.19
CUI: C0036572
Disease: Seizures
Seizures
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs3832300
rs3832300
1.000 0.040 4 47426318 3 prime UTR variant -/T delins 5.1E-02
CUI: C0036572
Disease: Seizures
Seizures
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs4482737
rs4482737
1.000 0.040 4 47320173 missense variant T/C;G snv 0.99; 4.0E-06
CUI: C0036572
Disease: Seizures
Seizures
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 < 0.001 1 2006 2006