Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 6 | |||
rs1535989 | 0.925 | 0.080 | 13 | 105370372 | intergenic variant | A/G;T | snv | 4 | |||
rs372032595 | 0.925 | 0.080 | 7 | 107904960 | missense variant | T/G | snv | 4.0E-06 | 3 | ||
rs189037 | 0.689 | 0.400 | 11 | 108223106 | 5 prime UTR variant | G/A | snv | 0.49 | 22 | ||
rs1065411 | 0.925 | 0.080 | 1 | 109690516 | missense variant | G/A;C;T | snv | 0.36; 6.9E-06 | 2 | ||
rs1805097 | 0.689 | 0.360 | 13 | 109782884 | missense variant | C/G;T | snv | 0.35 | 22 | ||
rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
rs3802842 | 0.695 | 0.280 | 11 | 111300984 | intron variant | C/A | snv | 0.71 | 25 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs201745983 | 0.752 | 0.200 | 12 | 111783219 | missense variant | G/A | snv | 6.8E-05 | 7.7E-05 | 14 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs12241008 | 0.716 | 0.160 | 10 | 112520943 | intron variant | T/C | snv | 0.13 | 16 | ||
rs10506868 | 0.716 | 0.160 | 10 | 112559621 | intron variant | C/T | snv | 3.1E-02 | 16 | ||
rs2295080 | 0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv | 20 | |||
rs79896135 | 0.925 | 0.080 | 5 | 112707585 | 5 prime UTR variant | C/A;G;T | snv | 2 | |||
rs11196067 | 0.752 | 0.160 | 10 | 112709306 | intron variant | A/T | snv | 0.32 | 10 | ||
rs7086803 | 0.763 | 0.160 | 10 | 112738717 | intron variant | G/A | snv | 0.20 | 9 | ||
rs150973053 | 0.851 | 0.200 | 5 | 112767356 | missense variant | A/G | snv | 3.5E-04 | 2.7E-04 | 4 | |
rs3783553 | 0.667 | 0.480 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 26 | |||
rs2856838 | 0.851 | 0.200 | 2 | 112782395 | intron variant | G/A | snv | 0.37 | 4 | ||
rs530670052 | 0.925 | 0.080 | 5 | 112801313 | missense variant | A/G | snv | 1.6E-05 | 1.4E-05 | 2 | |
rs454886 | 0.763 | 0.280 | 5 | 112810420 | intron variant | A/G | snv | 0.26 | 10 | ||
rs770649674 | 0.807 | 0.120 | 5 | 112827177 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 52 |