Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs2523477 0.925 0.080 6 31392612 downstream gene variant T/C snv 0.10 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs3128930 0.925 0.120 6 33107889 upstream gene variant C/T snv 0.31 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs1521 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 2
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 2
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2