Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs11514731
MAD1L1
1.000 0.040 7 2011868 intron variant C/G snv 0.16 2
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs11608355
MYO1H
1.000 0.040 12 109441487 intron variant T/C snv 0.33 2
rs116362708
SLC44A5
1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 2
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs11663393
DCC
1.000 0.040 18 53088362 intron variant G/A snv 0.40 2
rs11664123
DCC
1.000 0.040 18 53440658 intron variant T/C snv 0.24 2
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs1170191
DGKH
13 42101357 intron variant A/G;T snv 1
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs11826064 1.000 0.040 11 50818695 intergenic variant C/A;T snv 2
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12068879
KAZN
1.000 0.040 1 14959860 intron variant A/G snv 0.18 2
rs12137398
CAMTA1
1.000 0.040 1 7730488 intron variant C/T snv 0.14 2
rs12137936
NEGR1
1.000 0.040 1 72254674 intron variant C/G snv 0.23 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs12420205 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 2
rs12457157
TCF4
1.000 0.040 18 55629696 intron variant G/A snv 0.41 2
rs1261070
TCF4
1.000 0.040 18 55235854 intron variant A/G snv 0.94 2