Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs505974 0.882 0.080 3 190188984 intergenic variant T/C;G snv 4
rs568404 0.851 0.120 10 129233875 regulatory region variant C/A;G;T snv 4
rs7459185 0.851 0.160 7 76305323 downstream gene variant G/C;T snv 4
rs10508266 0.882 0.080 10 3797822 intergenic variant G/A;T snv 3
rs10512948 0.882 0.080 5 8233238 intron variant T/C snv 0.15 3
rs117781739 0.882 0.080 16 47835114 intron variant G/A;T snv 3
rs11878644 0.882 0.080 19 45373709 upstream gene variant T/C snv 0.53 3
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs13162612 0.882 0.080 5 8042908 intergenic variant A/G snv 5.1E-02 3
rs1560642 0.882 0.080 5 148888172 intergenic variant T/C;G snv 3
rs1663689 0.882 0.080 10 8983232 intergenic variant T/C snv 0.25 3
rs1814343 0.882 0.080 11 129695357 regulatory region variant C/T snv 0.22 3
rs2736107 0.882 0.080 5 1297739 upstream gene variant C/T snv 0.23 3
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 3
rs2924471 0.882 0.080 5 8055148 intergenic variant T/C snv 0.15 3
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs3742038 0.882 0.080 12 120371388 non coding transcript exon variant A/G snv 0.16 3
rs3856776 0.882 0.080 3 189580619 intergenic variant C/A;G;T snv 3
rs4665162 0.882 0.080 2 160203673 intron variant A/G snv 0.30 3