Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs12708967 16 56959299 upstream gene variant T/C snv 0.18 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs17410914 8 19985951 intergenic variant C/A;T snv 4
rs17411126 8 19997761 intergenic variant T/C snv 0.26 4
rs17489268 8 19994534 regulatory region variant T/A snv 0.25 4
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 4
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 4
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4