Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758946412
PCDH19
0.821 0.214 X 100407506 frameshift variant C/CG in-del 5.6E-06 12
rs869312825
GNB1
0.878 0.071 1 1804548 start lost T/C snp 11
rs869312826
GNB1
0.923 0.071 1 1787378 missense variant C/T snp 6
rs74315390
KCNQ2
0.744 0.107 20 63439609 missense variant C/G,T snp 5
rs121918622
LOC102724058 ; SCN1A
0.784 0.071 2 165992332 missense variant C/A,T snp 4.0E-06 3
rs121908918
LOC101929680 ; SCN9A
0.878 0.071 2 166284506 stop gained T/A snp 2.4E-05 2
rs1065852
LOC102723722 ; CYP2D6
0.756 0.250 22 42130692 missense variant G/A snp 0.21 0.19 2
rs118192250
KCNQ3
0.878 0.107 8 132175457 missense variant C/A snp 1