Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12520522 | 5 | 40494576 | intron variant | C/A;G;T | snv | 1 | |||||
rs1320959 | 6 | 135116248 | regulatory region variant | T/C | snv | 0.37 | 1 | ||||
rs17636351 | 12 | 59216246 | intergenic variant | C/G;T | snv | 1 | |||||
rs2326451 | 6 | 126490782 | intron variant | A/T | snv | 0.44 | 1 | ||||
rs554093579 | 7 | 100537063 | upstream gene variant | A/C | snv | 5.5E-03 | 1 | ||||
rs75225321 | 16 | 89672182 | non coding transcript exon variant | G/- | del | 0.23 | 1 | ||||
rs6430549 | 2 | 134858776 | intron variant | A/G | snv | 0.58 | 1 | ||||
rs10953299 | 7 | 100645788 | intron variant | T/C | snv | 0.21 | 1 | ||||
rs342437 | 4 | 87119757 | intron variant | A/G | snv | 0.65 | 1 | ||||
rs7311607 | 12 | 2413815 | intron variant | A/G | snv | 0.34 | 1 | ||||
rs7312105 | 12 | 2414189 | intron variant | A/G | snv | 0.34 | 1 | ||||
rs8100454 | 19 | 40820613 | intron variant | A/G | snv | 9.7E-02 | 1 | ||||
rs2742540 | 11 | 8877981 | intron variant | A/G | snv | 0.41 | 1 | ||||
rs8108461 | 19 | 2186758 | intron variant | T/C | snv | 0.55 | 1 | ||||
rs576195416 | 1 | 231374522 | intron variant | TT/-;T;TTT;TTTT;TTTTTTTTTTTT | delins | 1 | |||||
rs17400517 | 1 | 161515469 | intron variant | G/T | snv | 8.5E-02 | 1 | ||||
rs111843364 | 16 | 70923707 | intron variant | G/A | snv | 3.8E-02 | 1 | ||||
rs150522999 | X | 150167578 | intron variant | C/G | snv | 5.0E-02 | 1 | ||||
rs73736914 | 6 | 44010849 | intron variant | A/G | snv | 3.6E-02 | 1 | ||||
rs2032314 | 21 | 33982222 | downstream gene variant | T/C | snv | 0.86 | 1 | ||||
rs9273039 | 6 | 32644174 | non coding transcript exon variant | C/A;T | snv | 1 | |||||
rs151165225 | 19 | 45257662 | intron variant | C/T | snv | 0.19 | 1 | ||||
rs10711289 | 3 | 169450583 | intron variant | AAA/-;A;AA;AAAA;AAAAA | delins | 1 | |||||
rs138308793 | 2 | 111493181 | intron variant | G/A | snv | 0.11 | 1 | ||||
rs6442310 | 3 | 12316731 | intron variant | T/A | snv | 0.66 | 1 |