Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2268666
GRM1
1.000 0.040 6 146424952 intron variant C/T snv 0.51 1
rs772335034
P2RX2
1.000 0.040 12 132618851 missense variant C/A snv 9.6E-06 1
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 4
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3