Disease: Childhood Absence Epilepsy
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs1570624
EFHC1
0.882 0.040 6 52454252 missense variant G/A snv 1.0E-02 9.6E-03 3