Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs1345203
SOCAR ; MIR4435-2HG
2 111496274 intron variant T/C;G snv 2
rs16892496
TRHR
1.000 0.080 8 109097622 intron variant A/C;G;T snv 2
rs2194411 3 185830875 intergenic variant G/A;C snv 2
rs33966734
CCND3
6 41936060 stop gained C/A;G;T snv 1.2E-02; 4.0E-06 2
rs35320790
SALRNA1
14 60642107 intron variant C/A;G snv 2
rs622871
CYP21A2 ; C2
1.000 0.040 6 31910718 intron variant A/C;G snv 2
rs6762578
COPG1
3 129273204 intron variant G/A;T snv 2
rs7249081
AP3D1
19 2157168 intron variant T/C;G snv 2
rs74494415
GALR1
18 77260182 intron variant C/A;T snv 2
rs76307059
SMOC2
6 168600208 intron variant C/A;G;T snv 2
rs9843653 3 49883138 downstream gene variant T/A;C snv 2
rs11001398
LRMDA
10 75461756 intron variant G/A;C snv 1
rs11160601 14 100720304 regulatory region variant C/G;T snv 1
rs11200607
PLEKHA1
10 122395110 intron variant C/G;T snv 1
rs12907384
AKAP13
15 85732769 intron variant T/A;C snv 1
rs139055636 9 102796618 regulatory region variant C/A;T snv 1