Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1064797245
ATP1A3
0.776 0.280 19 41970540 missense variant G/A snv 12
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs796052676
KCNQ3
0.807 0.200 8 132180246 missense variant G/A snv 10
rs118192211
KCNQ2
0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs587776983
TUBB4A
0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
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
rs886041715
GNAO1 ; DKFZP434H168 ; LOC283856
0.827 0.040 16 56192353 missense variant G/A;C;T snv 7
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
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs222020
GC
0.851 0.320 4 71770555 intron variant C/T snv 0.72 5
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 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
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
rs1562902
CYP2R1
0.925 0.120 11 14896670 upstream gene variant C/T snv 0.55 3
rs796053150
SCN2A
1.000 0.040 2 165386827 missense variant A/G snv 3