Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 4
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 3
rs2871960
ZBTB38
3 141402972 5 prime UTR variant A/C snv 0.55 3
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3
rs13192994 6 75529546 intergenic variant A/C snv 0.10 1
rs185829646
ANKRD22
10 88823948 intron variant A/C snv 7.9E-04 1
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs780159
ZMIZ1
10 79147390 intron variant A/C;G snv 2
rs159544
SMIM15-AS1
5 61193420 intron variant A/C;G snv 1
rs743580
PML
15 74035775 missense variant A/C;G snv 0.52 1
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs6864049
LOC105379158 ; LINC02240
5 124994829 intron variant A/C;G;T snv 2
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs7550173
LOC105378797
1 72478934 intron variant A/C;T snv 2
rs1563352
LYPLAL1-AS1 ; LOC107985272
1 219479453 intergenic variant A/C;T snv 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6