Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs55799208 | 2 | 218135259 | missense variant | G/A | snv | 1.4E-03 | 1.4E-03 | 5 | |||
rs78487399 | 2 | 43582208 | intron variant | G/C | snv | 6.2E-02 | 5 | ||||
rs9287604 | 2 | 236867522 | intergenic variant | G/C | snv | 0.62 | 5 | ||||
rs10206089 | 2 | 61476184 | intron variant | G/A | snv | 4 | |||||
rs2029582 | 2 | 113106194 | upstream gene variant | T/C | snv | 0.56 | 4 | ||||
rs200476039 | 2 | 54760823 | intron variant | TTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT | delins | 5.5E-02 | 3 | ||||
rs7575217 | 2 | 101160470 | intron variant | A/G | snv | 0.68 | 3 | ||||
rs2860773 | 2 | 65438507 | intron variant | G/T | snv | 0.41 | 1 | ||||
rs6782228 | 3 | 128604581 | intergenic variant | G/C | snv | 0.28 | 7 | ||||
rs9819371 | 3 | 141487958 | intron variant | C/T | snv | 4.7E-02 | 5 | ||||
rs143699489 | 3 | 141208279 | intergenic variant | A/G | snv | 0.22 | 4 | ||||
rs11920354 | 3 | 47220756 | intron variant | C/A | snv | 0.34 | 3 | ||||
rs2734031 | 3 | 128582547 | intergenic variant | T/C | snv | 0.90 | 1 | ||||
rs9872440 | 3 | 42854959 | intron variant | T/C;G | snv | 1 | |||||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 23 | ||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs11725704 | 4 | 74094279 | downstream gene variant | A/G | snv | 0.28 | 5 | ||||
rs11734460 | 4 | 711285 | intron variant | C/A;T | snv | 4 | |||||
rs11931598 | 4 | 7045375 | intron variant | C/T | snv | 0.55 | 4 | ||||
rs1352846 | 4 | 71752058 | intron variant | A/G | snv | 0.22 | 4 | ||||
rs58548501 | 4 | 54635119 | intergenic variant | -/A;ATTTTTTTTTA | ins | 0.43 | 4 | ||||
rs28476539 | 4 | 82631138 | 3 prime UTR variant | G/A;T | snv | 3 | |||||
rs62312418 | 4 | 73835795 | upstream gene variant | G/A | snv | 0.34 | 3 | ||||
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 |