Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796053150
SCN2A
1.000 0.040 2 165386827 missense variant A/G snv 3
rs767399782
TUBB4A
0.925 0.120 19 6495736 missense variant C/A;T snv 4.0E-06 3
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
rs121918046
POLG
0.925 0.160 15 89325520 missense variant G/A snv 1.4E-05 4
rs222020
GC
0.851 0.320 4 71770555 intron variant C/T snv 0.72 5
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
rs756632799
LOC107985405 ; PIGT
0.882 0.080 20 45416579 stop gained G/T snv 1.6E-05 7.0E-06 5
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs527236031
PIGT ; MIR6812
0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs796052621
KCNQ2
0.827 0.080 20 63444756 missense variant C/T snv 6
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
rs1799821
CPT2
0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs2229291
CPT2
0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs118192211
KCNQ2
0.790 0.080 20 63439644 missense variant G/A;C snv 9