Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606621
AARS1
0.882 0.080 16 70268356 missense variant C/T snv 3
rs797044801
AARS1
1.000 0.080 16 70254688 missense variant T/G snv 1
rs1179887323
AARS2 ; TMEM151B
1.000 0.080 6 44307303 missense variant C/A;T snv 4.0E-06 1
rs73982299
ACACA
1.000 0.080 17 37274293 missense variant C/T snv 2.3E-04 9.3E-04 1
rs1037610094
ADRA1A
1.000 0.080 8 26864491 missense variant C/G;T snv 1.6E-05; 4.0E-06 1
rs9657362
ARHGEF10
0.882 0.120 8 1885635 missense variant G/C;T snv 0.16 3
rs17683288
ARHGEF10
0.925 0.080 8 1929314 missense variant T/G snv 5.4E-02 5.0E-02 2
rs2294039
ARHGEF10
0.925 0.080 8 1909425 missense variant G/A snv 3.1E-02 3.1E-02 2
rs587777712
ARHGEF10
1.000 0.080 8 1882687 missense variant G/A;C snv 1.8E-05 1
rs1553192091
ATP1A1 ; ATP1A1-AS1
0.925 0.080 1 116395247 missense variant C/A;G snv 2
rs121918312
BAG3
0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 13
rs113994102
CTDP1
0.925 0.160 18 79710825 intron variant C/T snv 2
rs776497952
DHTKD1
1.000 0.080 10 12117722 missense variant C/A;T snv 2.4E-05 1
rs730882139
DNAJB2
0.925 0.080 2 219281772 splice donor variant G/A snv 2
rs730882140
DNAJB2
0.925 0.080 2 219279847 missense variant A/G snv 2
rs121909088
DNM2
0.925 0.080 19 10819992 missense variant A/G snv 3
rs267606772
DNM2
0.925 0.080 19 10793799 missense variant G/A snv 3
rs199927590
DNM2
1.000 0.080 19 10797424 missense variant A/G snv 1.1E-04 1.0E-04 1
rs387906738
DYNC1H1
0.882 0.080 14 101980506 missense variant A/G snv 3
rs587781253
DYNC1H1
1.000 0.080 14 101985925 missense variant G/A snv 4.0E-06 1
rs104894161
EGR2
0.807 0.080 10 62813563 missense variant G/A snv 6
rs104894158
EGR2
0.851 0.080 10 62813835 missense variant A/T snv 5
rs104894159
EGR2
0.827 0.080 10 62813413 missense variant G/A snv 5
rs281865137
EGR2
0.851 0.080 10 62813496 missense variant C/T snv 4