Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10261878 7 25910925 intergenic variant A/C snv 0.80 1
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 1
rs1106683 7 131768766 intergenic variant G/A snv 0.14 1
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 1
rs12597579 16 20246545 intergenic variant C/A;T snv 1
rs12964056 18 60006567 upstream gene variant A/G;T snv 1
rs13396935 2 653195 intergenic variant G/A snv 0.18 1
rs1555543 1 96479241 intergenic variant A/C snv 0.55 1
rs16858082 4 45173787 intergenic variant T/C snv 0.41 1
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 1
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 1
rs2867112 2 651349 intergenic variant T/G snv 0.18 1
rs2890652 2 142202362 intergenic variant T/C snv 0.21 1
rs2903492 2 624678 intergenic variant G/A snv 0.85 1
rs2922763 8 75661476 intergenic variant G/T snv 0.77 1
rs348495 4 45182425 intergenic variant G/A snv 0.49 1
rs4854349 2 647861 intergenic variant T/C snv 0.77 1
rs516636 1 177886382 intron variant C/A snv 0.17 1
rs574367 1 177904075 intron variant G/T snv 0.16 1
rs591166 18 60174356 intergenic variant T/A snv 0.52 1
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 1
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 1
rs867559 9 126703046 non coding transcript exon variant A/G snv 0.26 1
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 1
rs9473924 6 50866444 intergenic variant G/T snv 0.33 1