Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 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
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs116009877 6 25715429 regulatory region variant G/A;T snv 4
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 4
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 4
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 4
rs1558861 11 116736721 regulatory region variant C/G;T snv 4
rs176813 4 68733813 regulatory region variant T/C snv 0.38 4
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2954022 8 125470379 intron variant C/A;T snv 4