Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs16858082 4 45173787 intergenic variant T/C snv 0.41 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 2
rs2890652 2 142202362 intergenic variant T/C snv 0.21 2
rs2903492 2 624678 intergenic variant G/A snv 0.85 2
rs2922763 8 75661476 intergenic variant G/T snv 0.77 2
rs2941428 0.925 0.120 8 75613351 intergenic variant G/A snv 0.66 2
rs348495 4 45182425 intergenic variant G/A snv 0.49 2