Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10018902 | 4 | 120941346 | intergenic variant | G/A;T | snv | 1 | |||||
rs12517906 | 5 | 180743819 | upstream gene variant | C/A;T | snv | 0.11 | 1 | ||||
rs12705992 | 7 | 114789947 | regulatory region variant | G/A | snv | 0.72 | 1 | ||||
rs13029479 | 2 | 655222 | regulatory region variant | G/A | snv | 0.13 | 1 | ||||
rs151204774 | 11 | 21580341 | downstream gene variant | AATT/- | delins | 7.4E-02 | 1 | ||||
rs17668565 | 5 | 92818872 | intergenic variant | T/A;C | snv | 1 | |||||
rs182624399 | 11 | 70019090 | intron variant | C/T | snv | 8.9E-03 | 1 | ||||
rs1840440 | 18 | 25677222 | intergenic variant | T/C;G | snv | 1 | |||||
rs1973993 | 1 | 96478438 | intergenic variant | T/C | snv | 0.49 | 1 | ||||
rs630372 | 1 | 177916627 | intron variant | G/A;T | snv | 1 | |||||
rs6440919 | 3 | 153982187 | upstream gene variant | C/T | snv | 0.47 | 1 | ||||
rs6735049 | 2 | 630569 | intergenic variant | T/A;C | snv | 1 | |||||
rs6780892 | 3 | 7947364 | downstream gene variant | G/A;T | snv | 1 | |||||
rs72989246 | 18 | 60053966 | TF binding site variant | C/T | snv | 8.1E-02 | 1 | ||||
rs73144267 | 7 | 76923428 | downstream gene variant | T/C | snv | 0.23 | 1 | ||||
rs7336332 | 13 | 27484267 | upstream gene variant | A/G | snv | 0.19 | 1 | ||||
rs7777593 | 7 | 36506461 | downstream gene variant | T/A;G | snv | 1 | |||||
rs80116344 | 18 | 60281167 | intergenic variant | G/A | snv | 3.9E-02 | 1 | ||||
rs9313296 | 5 | 165950694 | intergenic variant | G/C | snv | 0.13 | 1 | ||||
rs16877106 | 4 | 25401644 | intron variant | C/T | snv | 4.9E-02 | 1 | ||||
rs112037309 | 4 | 105695979 | intron variant | G/A | snv | 6.7E-02 | 1 | ||||
rs6416056 | 11 | 27625198 | intron variant | G/A | snv | 0.71 | 1 | ||||
rs534356339 | 4 | 91335712 | intron variant | GAT/- | del | 3.4E-03 | 1 | ||||
rs494558 | 13 | 110276815 | intron variant | C/T | snv | 0.90 | 1 | ||||
rs286028 | 11 | 85394069 | intron variant | A/C;T | snv | 1 |