Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs62200793 0.925 0.040 2 184885915 intron variant T/C snv 0.15 2
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs74796725 0.882 0.040 12 53187599 3 prime UTR variant G/T snv 1.2E-02 1.3E-02 3
rs1715 0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs62110082 1.000 0.040 19 51835388 intron variant T/C snv 4.1E-02 2
rs9393813 1.000 0.040 6 27363817 upstream gene variant C/A;T snv 1
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs11557713 1.000 0.040 18 62576643 3 prime UTR variant G/A snv 0.25 1
rs139459337 0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs149268645 0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs6738485 0.882 0.040 2 106193504 intron variant C/T snv 0.36 3
rs7219021 0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs1705236 0.827 0.200 12 71151778 intron variant T/A snv 7.6E-02 1
rs116403057 1.000 0.040 6 32335895 intron variant T/A snv 1
rs3818253 1.000 0.040 20 35009073 intron variant G/A snv 0.19 3
rs79436609 1.000 0.040 3 140698604 intron variant T/C snv 1.8E-02 2
rs2021722 0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs3732386 0.925 0.040 3 36830502 intron variant C/T snv 0.38 2
rs11129735 1.000 0.040 3 36828739 intron variant A/G snv 0.53 1
rs11706780 1.000 0.040 3 36854744 intron variant C/T snv 0.36 1
rs12637912 1.000 0.040 3 36830403 intron variant C/A snv 0.27 1
rs17807744 1.000 0.040 3 36852557 intron variant C/T snv 0.36 1
rs4234258 1.000 0.040 3 36837479 intron variant A/G snv 0.40 1