Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 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
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
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
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 4