Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 5