Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8083296 0.925 0.040 18 6158717 intron variant A/C snv 5.4E-02 2
rs9906298 0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 2
rs4245791 0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs6756629 0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 2
rs41360247 0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 2
rs4149000 0.882 0.080 12 21295063 non coding transcript exon variant C/T snv 0.11 2
rs4299376 0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs2241423 0.882 0.120 15 67794500 intron variant G/A snv 0.29 2
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 3
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs4148217 0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 3
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5