Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs10884216 0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs11082011 0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11155372 0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs112106319 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs116609693 0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs11728985 0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11990063 0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 1
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs139438618 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4