Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 4
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs198833 6 26114280 downstream gene variant G/A snv 0.87 4
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs668459 6 139514552 intron variant C/T snv 0.51 4
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs592423 6 139519556 intron variant A/C snv 0.50 3
rs5994574 22 32470947 upstream gene variant T/C snv 0.46 3
rs632057 6 139512875 intron variant T/G snv 0.57 3
rs7757054 6 135166476 intergenic variant A/G snv 0.13 3
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs172629 4 54541595 intergenic variant C/G snv 0.17 2
rs218238 4 54528857 intergenic variant A/T snv 0.38 2
rs218256 4 54536242 intergenic variant C/G snv 0.38 2
rs2340727 1 161976937 intergenic variant A/G snv 0.33 2
rs628751 6 139517282 intron variant C/A snv 0.41 2