Disease: EPILEPSY, BENIGN NEONATAL, 2
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118192211
KCNQ2
0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs74315392
KCNQ2
0.851 0.080 20 63442482 stop gained G/A;C;T snv 4
rs118192235
KCNQ2 ; LOC105372724
0.882 0.080 20 63413471 missense variant C/A;T snv 3
rs267607198
LOC105372724 ; KCNQ2
0.882 0.080 20 63413551 missense variant C/A;T snv 3