Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4713226
UBDP1
1.000 0.120 6 29466637 intron variant G/A;T snv 2
rs10195263 2 150869278 intergenic variant G/A;C snv 1
rs10489759 1 189620209 regulatory region variant C/T snv 0.17 1
rs10512697 5 3558424 intergenic variant T/C snv 5.3E-02 1
rs12256830 10 53624983 intergenic variant C/T snv 5.5E-02 1
rs12775535 10 25629950 intergenic variant C/T snv 2.9E-02 1
rs1322846 6 17240923 intron variant T/C snv 0.39 1
rs1403155 1.000 0.120 7 68585426 intergenic variant G/A snv 2.9E-02 1
rs17007761 2 122468047 intron variant C/A snv 6.0E-02 1
rs17142462 7 119966578 intergenic variant C/A;T snv 1
rs2043599 19 55939683 intergenic variant A/G snv 5.9E-02 1
rs381365 X 146667390 intergenic variant T/G snv 1
rs4469412 8 33707860 intron variant G/A snv 5.8E-02 1
rs6576443 15 25649511 intergenic variant C/T snv 0.42 1
rs7140601 14 97996820 regulatory region variant T/A;C snv 1
rs7394570 11 42294336 intergenic variant A/G snv 0.89 1
rs859267 17 15922707 intergenic variant A/C;G snv 1
rs9807334 1.000 0.080 18 50997791 intron variant G/A snv 6.6E-02 1
rs9835812 3 3334100 intron variant G/A;T snv 1
rs12148329
ABHD17C
15 80708937 intron variant T/G snv 0.13 1
rs7658486
ARHGAP10
4 147963038 intron variant C/T snv 7.5E-02 1
rs10517025
ATP8A1
4 42451236 intron variant C/T snv 0.15 1
rs7105056
BCO2
11 112193708 non coding transcript exon variant T/C snv 0.97 0.95 1
rs2255327
BLK
8 11552483 intron variant C/T snv 1.2E-02 1
rs2501276
CDC42-AS1 ; CDC42
1 22047131 intron variant C/T snv 8.1E-02 1