Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs189010983 | 1.000 | 0.040 | 12 | 83692397 | intergenic variant | C/A;T | snv | 1.4E-02 | 1 | ||
rs190797076 | 1.000 | 0.040 | 4 | 110589931 | intergenic variant | G/A;T | snv | 9.7E-03 | 1 | ||
rs1955873 | 1.000 | 0.040 | 14 | 25573788 | intergenic variant | A/G | snv | 0.97 | 1 | ||
rs201958930 | 1.000 | 0.040 | 4 | 58871307 | intron variant | AAA/-;AA;AAAA | delins | 1 | |||
rs209345 | 1.000 | 0.040 | 5 | 162064381 | intron variant | T/C;G | snv | 1 | |||
rs6092354 | 1.000 | 0.040 | 20 | 56719418 | intergenic variant | G/T | snv | 7.5E-02 | 1 | ||
rs6708110 | 1.000 | 0.040 | 2 | 4007215 | intergenic variant | G/C | snv | 6.4E-02 | 1 | ||
rs71370433 | 1.000 | 0.040 | 17 | 6294504 | intergenic variant | C/T | snv | 1.3E-02 | 1 | ||
rs73078593 | 1.000 | 0.040 | 20 | 12310875 | intron variant | C/A | snv | 4.1E-02 | 1 | ||
rs73126576 | 1.000 | 0.040 | 20 | 39961687 | regulatory region variant | T/C | snv | 2.9E-02 | 1 | ||
rs73989024 | 1.000 | 0.040 | 17 | 49932105 | intron variant | A/G | snv | 5.5E-02 | 1 | ||
rs74852193 | 1.000 | 0.040 | 1 | 68698339 | non coding transcript exon variant | G/A | snv | 3.8E-02 | 1 | ||
rs76065397 | 1.000 | 0.040 | 15 | 35904724 | intergenic variant | T/C | snv | 1.8E-02 | 1 | ||
rs78606339 | 1.000 | 0.040 | 5 | 166001974 | intergenic variant | T/A | snv | 5.7E-02 | 1 | ||
rs79947075 | 1.000 | 0.040 | 17 | 40764791 | downstream gene variant | C/T | snv | 9.5E-03 | 1 | ||
rs80017116 | 1.000 | 0.040 | 3 | 150064125 | intron variant | G/A | snv | 5.6E-03 | 1 | ||
rs76745467 | 1.000 | 0.040 | 14 | 68959672 | intron variant | C/T | snv | 2.4E-02 | 1 | ||
rs78277363 | 1.000 | 0.040 | 5 | 7627129 | intron variant | A/G | snv | 1.7E-02 | 1 | ||
rs13133980 | 1.000 | 0.040 | 4 | 41000929 | intron variant | G/A;C;T | snv | 1 | |||
rs1216578110 | 1.000 | 0.040 | 21 | 25955652 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs75316710 | 1.000 | 0.040 | 3 | 10508052 | intron variant | A/G | snv | 2.9E-02 | 1 | ||
rs77609452 | 1.000 | 0.040 | 8 | 26454581 | intron variant | G/A | snv | 2.3E-02 | 1 | ||
rs12628463 | 1.000 | 0.040 | 22 | 19401286 | intron variant | C/A | snv | 6.2E-03 | 1 | ||
rs79158673 | 1.000 | 0.040 | 3 | 62457132 | intron variant | G/A | snv | 1.1E-02 | 1 | ||
rs799979 | 1.000 | 0.040 | 7 | 80415882 | intron variant | A/G | snv | 2.7E-02 | 1 |