Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 3
rs4718789 0.925 0.120 7 68579188 intergenic variant C/T snv 8.1E-02 2
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs227959 1.000 0.040 17 3406923 upstream gene variant C/T snv 1
rs4829605 1.000 0.040 X 137182822 intergenic variant C/A;G snv 1
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1451603364
BDNF-AS ; BDNF
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs774321998
C1orf167 ; MTHFR
1.000 0.040 1 11790683 missense variant T/C snv 4.0E-06 7.0E-06 1
rs3756577
CAMK2A
0.925 0.080 5 150249081 intron variant C/T snv 0.14 2
rs3822606
CAMK2A
0.925 0.080 5 150261592 intron variant G/A snv 0.27 2
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68