Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17513613 19 29795915 regulatory region variant T/C snv 0.25 2
rs17568628 5 76751114 intergenic variant T/C;G snv 2
rs17738166 5 173570975 intron variant G/A;C snv 2
rs2357760 6 119892734 intergenic variant G/A;C snv 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs36061954 8 38472132 upstream gene variant C/T snv 0.34 2
rs4580892 6 127088737 intron variant C/T snv 0.32 2
rs4722530 7 25844482 regulatory region variant G/T snv 0.24 2
rs6130360 20 43382356 intergenic variant A/G snv 0.19 2
rs622217 1.000 0.080 6 160345738 upstream gene variant T/A;C snv 2
rs6725549 2 630323 intergenic variant C/A snv 0.85 2
rs704061 12 89378126 intron variant T/C snv 0.49 2
rs7231852 18 43182011 intergenic variant G/A;T snv 2
rs10024899 4 121705035 intergenic variant T/C snv 0.35 1
rs10070064 5 173854774 intergenic variant C/T snv 0.26 1
rs10458575 1 65104082 regulatory region variant T/C snv 0.45 1
rs10464079 5 179098778 intergenic variant G/A snv 0.71 1
rs10475249 5 4010021 downstream gene variant C/G snv 0.45 1
rs10490869 3 35593653 intergenic variant A/T snv 0.15 1
rs10501039 11 26152856 intergenic variant T/C snv 4.5E-02 1
rs10507223 12 108062051 intergenic variant C/G snv 0.17 1
rs10763957 10 33877770 regulatory region variant C/T snv 0.35 1
rs10827252 10 33383956 upstream gene variant A/G snv 0.51 1
rs10844642 12 33577433 downstream gene variant A/C snv 0.27 1
rs10851523 15 52751805 downstream gene variant G/A;C snv 1