Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3820422
CACNA1S
1.000 0.040 1 201076345 intron variant A/G snv 0.25 1
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs589249
LOC105378648 ; LOC107984941
1.000 0.040 1 36696751 intergenic variant A/G;T snv 1
rs6427339
ARHGEF11
1.000 0.040 1 156984475 intron variant C/T snv 0.47 0.50 1
rs6427340
ARHGEF11
0.925 0.120 1 156984592 intron variant T/C snv 0.46 1
rs6681578
CACHD1
1.000 0.040 1 64547903 intron variant T/C snv 0.59 1
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 1
rs6703335
SDCCAG8
0.882 0.040 1 243445665 intron variant A/G snv 0.50 1
rs7527939
HHAT
1.000 0.040 1 210362681 intron variant C/T snv 0.30 1
rs7544736 1.000 0.040 1 96698787 upstream gene variant A/G snv 0.22 1
rs7550594
LOC105378714 ; DMRTA2
1.000 0.040 1 50425421 upstream gene variant C/G;T snv 1
rs7550768 1.000 0.040 1 11620226 upstream gene variant C/T snv 0.82 1
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1
rs12052937
LRRFIP1
1.000 0.040 2 237637929 intron variant C/T snv 0.25 1
rs12463773
GTDC1
1.000 0.040 2 144150663 intron variant T/A snv 6.1E-02 1
rs12991836
ZEB2
1.000 0.040 2 144383974 intron variant A/C;T snv 1
rs13008971 1.000 0.040 2 8840342 upstream gene variant A/C snv 0.58 1
rs13025591
AGAP1
1.000 0.040 2 235886699 intron variant A/C snv 0.37 1
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1477450 1.000 0.040 2 117690910 intergenic variant G/A snv 0.41 1
rs17180327 1.000 0.040 2 180151406 intergenic variant A/G snv 0.25 1