Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1568952 | 1.000 | 0.080 | 8 | 58799804 | intergenic variant | T/C | snv | 0.75 | 1 | ||
rs6507226 | 1.000 | 0.080 | 18 | 22611328 | intergenic variant | A/G | snv | 0.45 | 1 | ||
rs9271300 | 1.000 | 0.080 | 6 | 32613805 | intergenic variant | C/G | snv | 0.54 | 1 | ||
rs3092923 | 1.000 | 0.080 | X | 136659026 | intron variant | T/C | snv | 0.17 | 0.28 | 1 | |
rs10841847 | 1.000 | 0.080 | 12 | 8535216 | intron variant | A/G | snv | 0.58 | 1 | ||
rs15493 | 1.000 | 0.080 | 14 | 67651415 | missense variant | C/G;T | snv | 9.2E-02 | 8.8E-02 | 1 | |
rs9272461 | 1.000 | 0.080 | 6 | 32637832 | intron variant | G/A | snv | 0.13 | 1 | ||
rs2230424 | 1.000 | 0.080 | 16 | 31355997 | missense variant | T/C | snv | 8.6E-02 | 9.0E-02 | 1 | |
rs2660898 | 1.000 | 0.080 | 12 | 96032219 | intron variant | T/G | snv | 0.30 | 1 | ||
rs1371562 | 1.000 | 0.080 | 2 | 118975372 | intron variant | G/T | snv | 0.33 | 1 | ||
rs17009726 | 1.000 | 0.080 | 2 | 118967884 | intron variant | A/G | snv | 1.0E-02 | 1 | ||
rs17795618 | 1.000 | 0.080 | 2 | 118973892 | intron variant | T/A | snv | 0.12 | 1 | ||
rs2011839 | 1.000 | 0.080 | 2 | 118985008 | intron variant | C/A;T | snv | 1 | |||
rs2278589 | 1.000 | 0.080 | 2 | 118971300 | intron variant | G/A;C | snv | 1 | |||
rs6761637 | 1.000 | 0.080 | 2 | 118981487 | missense variant | T/C | snv | 8.3E-02 | 0.13 | 1 | |
rs3774275 | 1.000 | 0.080 | 3 | 187247480 | intron variant | A/G | snv | 0.22 | 1 | ||
rs11575886 | 1.000 | 0.080 | 20 | 56248494 | upstream gene variant | A/G | snv | 8.0E-02 | 1 | ||
rs9905742 | 1.000 | 0.080 | 17 | 4539780 | missense variant | T/A | snv | 3.0E-02 | 2.7E-02 | 1 | |
rs1050504 | 1.000 | 0.080 | 8 | 58583857 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
rs208290 | 1.000 | 0.080 | 12 | 121156253 | intron variant | G/A | snv | 0.43 | 1 | ||
rs656612 | 1.000 | 0.080 | 12 | 121138849 | intron variant | C/A | snv | 0.60 | 1 | ||
rs1057141 | 1.000 | 0.080 | 6 | 32850997 | missense variant | T/C | snv | 0.20 | 0.20 | 1 | |
rs3859664 | 1.000 | 0.080 | 20 | 3691244 | intron variant | G/A | snv | 0.34 | 1 | ||
rs10208770 | 1.000 | 0.080 | 2 | 230170151 | intron variant | T/G | snv | 0.14 | 1 | ||
rs10498244 | 1.000 | 0.080 | 2 | 230173117 | non coding transcript exon variant | T/C | snv | 0.26 | 1 |