Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11168936 0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 15
rs41293497 0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 14
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs121913294 0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 11
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 11
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 11
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 11
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10