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
rs121909673
GABRG2
0.776 0.080 5 162093965 missense variant G/A snv 10
rs25409
LOC112268151 ; GABRB3
0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03 4
rs267606697
CACNA1H
0.925 0.040 16 1204325 missense variant G/A snv 2.4E-04 4.2E-05 3
rs8044363
CACNA1H
0.925 0.040 16 1200559 synonymous variant T/A;C snv 0.37 3
rs1570624
EFHC1
0.882 0.040 6 52454252 missense variant G/A snv 1.0E-02 9.6E-03 3
rs373363000
GABRA6
0.882 0.080 5 161686327 missense variant C/A;T snv 4.0E-06; 3.3E-04 3
rs71651682
GABRB3 ; LOC112268151
0.925 0.040 15 26772759 missense variant C/T snv 3
rs9934839
CACNA1H
0.925 0.040 16 1202259 synonymous variant A/G snv 0.42 0.50 2
rs10462087
HCN1
0.925 0.040 5 45295178 intron variant T/C snv 5.5E-02 2
rs1053074
KCNJ10
0.925 0.040 1 160039331 3 prime UTR variant A/C snv 0.46 2
rs12729701
KCNJ10
0.925 0.040 1 160042616 intron variant A/G snv 0.19 2
rs371775791
NIPA2
0.925 0.040 15 22866495 missense variant A/G snv 7.2E-05 5.6E-05 2