Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 2
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 2
rs6568421 1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23 2
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 2
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 2
rs10521318 16 85977731 intron variant C/G;T snv 1
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 1
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 1
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 1
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 1
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 1
rs13204742 1.000 0.040 6 127924620 intergenic variant G/T snv 9.3E-02 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs1505992 5 40498475 intron variant A/T snv 0.61 1
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 1
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 1
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 1
rs1819333 1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57 1
rs1819658 1.000 0.040 10 58153390 regulatory region variant C/G;T snv 1
rs194749 1.000 0.040 14 68807188 intergenic variant T/C snv 0.23 1
rs2097432 1.000 0.040 6 32622994 TF binding site variant T/C snv 0.27 1
rs2472649 4 73991991 upstream gene variant A/G;T snv 1
rs2651244 1.000 0.040 1 70529879 upstream gene variant G/A snv 0.30 1
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 1