Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 3
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs10508503 1.000 0.080 10 16257952 intergenic variant C/A;T snv 2
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 2
rs1013443 5 180774114 intergenic variant A/T snv 1.4E-03 1
rs10958725 8 42669441 intergenic variant T/G snv 0.63 1
rs10958726 8 42680766 intergenic variant G/T snv 0.66 1
rs11071927 15 66968834 intergenic variant C/A snv 0.85 1
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs12461383 19 40864433 intron variant C/G snv 0.42 1
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 1
rs1383634 15 78737054 downstream gene variant T/C snv 0.53 1