Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs745386663
GLB1
0.807 0.160 3 33051956 missense variant G/A snv 8.0E-06 2.1E-05 7
rs886041715
GNAO1 ; DKFZP434H168 ; LOC283856
0.827 0.040 16 56192353 missense variant G/A;C;T snv 7
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs796052621
KCNQ2
0.827 0.080 20 63444756 missense variant C/T snv 6
rs1162306056
KCNQ3
0.882 0.080 8 132174294 missense variant C/T snv 5
rs121918807
LOC102724058 ; SCN1A ; SCN1A-AS1
0.851 0.080 2 165994275 missense variant G/A snv 7.2E-05 2.8E-05 5
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs527236031
PIGT ; MIR6812
0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5
rs121918046
POLG
0.925 0.160 15 89325520 missense variant G/A snv 1.4E-05 4
rs281864720
ALK
0.925 0.040 2 29213994 missense variant A/C;G;T snv 4
rs368311455
CPT2
0.882 0.200 1 53211185 missense variant C/T snv 3.2E-05 2.8E-05 4
rs796052650
LOC105372724 ; KCNQ2
0.925 0.040 20 63413574 missense variant G/A;C snv 4
rs1057518443
CUL4B
1.000 0.040 X 120557964 missense variant T/C snv 3
rs1057524792
LIAS
1.000 0.040 4 39467617 missense variant T/G snv 3
rs751866383
LIAS
1.000 0.040 4 39470047 missense variant G/T snv 4.0E-06 3
rs767399782
TUBB4A
0.925 0.120 19 6495736 missense variant C/A;T snv 4.0E-06 3
rs771844443
SCN2A
1.000 0.040 2 165309194 missense variant A/G snv 4.0E-06 3
rs796053150
SCN2A
1.000 0.040 2 165386827 missense variant A/G snv 3
rs866291718
LIAS
1.000 0.040 4 39470042 missense variant A/G snv 3
rs961150638
LIAS
1.000 0.040 4 39470038 missense variant G/C snv 4.0E-06 3
rs1057518694
YARS2 ; DNM1L
1.000 12 32731069 missense variant G/A snv 2
rs1060499537
KCNT2
1.000 1 196429676 missense variant A/T snv 2
rs118192205
KCNQ2
1.000 20 63442495 missense variant G/A snv 2
rs1554616628
YWHAG
1.000 7 76329927 missense variant G/A snv 2