Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs11021221 11 95575690 intron variant T/A;G snv 4
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs778387 1 56158423 intron variant C/A;G;T snv 4
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs35259020 9 134085798 intergenic variant CT/- delins 0.18 3
rs875741 5 173860848 intergenic variant G/A;C snv 3
rs1203833 16 168533 upstream gene variant T/C snv 0.21 2
rs2145943 20 39934603 upstream gene variant A/C;G snv 2
rs35788208 5 154654616 intergenic variant C/T snv 7.4E-02 2
rs3748136 8 9172650 intron variant G/A snv 0.21 2
rs4728335 7 134697578 regulatory region variant G/C snv 0.33 2
rs74417235 5 154647656 intergenic variant A/G snv 7.3E-02 2
rs10067881 5 95826771 upstream gene variant G/A snv 9.4E-02 1
rs10449752 1 56152275 intron variant T/A;G snv 1
rs10710459 1 56467292 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA;AAAAAAAA delins 0.87 1