Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs200764640 | 0.925 | 0.080 | 7 | 99666641 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs34662244 | 0.925 | 0.120 | 6 | 28106103 | intron variant | G/A | snv | 5.0E-02 | 2 | ||
rs13054095 | 1.000 | 0.080 | 22 | 29010231 | intron variant | A/T | snv | 1.6E-02 | 1 | ||
rs62235753 | 1.000 | 0.080 | 22 | 28876649 | intergenic variant | C/T | snv | 1.3E-02 | 1 | ||
rs1190999960 | 0.807 | 0.240 | 11 | 65571690 | missense variant | G/A | snv | 9 | |||
rs3094146 | 1.000 | 0.080 | 6 | 30003183 | non coding transcript exon variant | G/C | snv | 6.1E-02 | 1 | ||
rs8113308 | 0.925 | 0.080 | 19 | 51942133 | intron variant | T/C | snv | 0.24 | 2 | ||
rs3810151 | 0.925 | 0.080 | 19 | 42224684 | missense variant | T/C | snv | 0.11 | 7.7E-02 | 2 | |
rs375066 | 1.000 | 0.080 | 19 | 43919418 | intron variant | T/A;C | snv | 1 | |||
rs9940645 | 0.925 | 0.080 | 16 | 49797677 | intron variant | A/G | snv | 0.54 | 2 | ||
rs10235235 | 0.925 | 0.080 | 7 | 99478208 | intron variant | T/C | snv | 0.13 | 4 | ||
rs143072280 | 1.000 | 0.080 | 10 | 38105003 | intron variant | -/CTTT | delins | 0.40 | 1 | ||
rs16917302 | 0.851 | 0.080 | 10 | 62501439 | intron variant | A/C | snv | 0.18 | 5 | ||
rs10822013 | 0.851 | 0.080 | 10 | 62492218 | intron variant | C/T | snv | 0.42 | 4 | ||
rs10995190 | 0.882 | 0.080 | 10 | 62518923 | intron variant | G/A | snv | 0.16 | 4 | ||
rs10995201 | 1.000 | 0.080 | 10 | 62540131 | intron variant | A/G | snv | 0.16 | 1 | ||
rs4986771 | 0.925 | 0.080 | 19 | 51965039 | missense variant | A/G | snv | 3.1E-02 | 2.7E-02 | 2 | |
rs2278415 | 0.925 | 0.080 | 19 | 51964950 | missense variant | T/A | snv | 0.16 | 0.14 | 2 | |
rs2278420 | 0.925 | 0.080 | 19 | 51968619 | missense variant | A/G | snv | 0.20 | 0.24 | 2 | |
rs8109631 | 0.882 | 0.080 | 19 | 53576890 | synonymous variant | A/G | snv | 0.70 | 0.76 | 3 | |
rs34196306 | 1.000 | 0.080 | 6 | 27457865 | intron variant | G/C | snv | 4.7E-02 | 1 | ||
rs704010 | 0.851 | 0.080 | 10 | 79081391 | intron variant | T/C | snv | 0.71 | 4 | ||
rs1250009 | 0.925 | 0.080 | 10 | 79085654 | intron variant | G/A;C | snv | 2 | |||
rs1268974 | 1.000 | 0.080 | 10 | 79092621 | intron variant | A/G | snv | 0.65 | 1 | ||
rs13214023 | 1.000 | 0.080 | 6 | 28364364 | intron variant | G/A | snv | 5.2E-02 | 1 |