Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
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
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 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
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
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
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8