Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs1822534 3 12225304 intergenic variant A/G;T snv 2
rs58106596 2 231714669 downstream gene variant G/A;C snv 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs10243593 7 39932526 intergenic variant G/A snv 0.44 1
rs10844639 12 9736166 upstream gene variant C/T snv 0.31 1
rs112158604 1 150724317 upstream gene variant GCTTCTGCA/- delins 1
rs113924863 6 32615369 regulatory region variant C/T snv 1
rs11676298 2 226427015 intergenic variant C/G snv 0.14 1
rs11779535 8 100376055 downstream gene variant G/A;C;T snv 1
rs12139775 1 198625652 intergenic variant C/T snv 6.3E-02 1
rs13230583 7 150620190 intergenic variant T/A;C snv 1
rs1333054 9 22165584 regulatory region variant C/T snv 0.36 1
rs151205200 5 158559574 intron variant TTACATT/-;TTACATTTTACATT delins 0.24 1
rs1586459 4 38312549 intergenic variant A/G snv 0.85 1
rs1861090 12 9777083 intergenic variant A/G snv 0.34 1
rs2224234 14 102915701 downstream gene variant A/C snv 0.33 1
rs2326837 6 6901426 non coding transcript exon variant A/G snv 0.31 1
rs2524035 6 29864555 intron variant A/G snv 0.81 1
rs28599891 6 32484693 intergenic variant C/G snv 0.63 1
rs35251378 19 10349293 downstream gene variant G/A snv 0.24 1
rs369457490 9 137038609 intron variant TAAATAAATAAATAAATAAA/-;TAAA;TAAATAAA;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAA delins 1