Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs59901009 | 11 | 10156890 | intron variant | T/C | snv | 0.25 | 2 | ||||
rs568645819 | 11 | 10228118 | intron variant | TTGT/- | delins | 2 | |||||
rs66803065 | 11 | 10004305 | intron variant | C/A;T | snv | 0.19 | 2 | ||||
rs17368443 | 11 | 10275289 | intron variant | G/C | snv | 5.3E-02 | 1 | ||||
rs4323860 | 11 | 10138336 | intron variant | T/C | snv | 0.50 | 1 | ||||
rs11042662 | 11 | 10193627 | intron variant | C/T | snv | 0.27 | 1 | ||||
rs55893317 | 11 | 10159444 | intron variant | A/G | snv | 0.25 | 1 | ||||
rs75248620 | 11 | 9887580 | intron variant | G/A | snv | 5.5E-02 | 1 | ||||
rs12361687 | 11 | 9868505 | intron variant | G/A | snv | 0.27 | 1 | ||||
rs360124 | 11 | 9780681 | non coding transcript exon variant | G/C | snv | 0.88 | 1 | ||||
rs2220970 | 11 | 9836202 | intron variant | G/A | snv | 0.80 | 1 | ||||
rs10840349 | 11 | 10054883 | intron variant | A/G;T | snv | 1 | |||||
rs7122422 | 11 | 10045715 | intron variant | G/C | snv | 0.37 | 1 | ||||
rs1470260 | 11 | 10253573 | intron variant | T/C | snv | 0.20 | 1 | ||||
rs117518788 | 11 | 9980672 | intron variant | C/T | snv | 2.9E-02 | 1 | ||||
rs418635 | 0.925 | 0.040 | 11 | 9796458 | intron variant | T/C | snv | 6.6E-02 | 2 | ||
rs1372812 | 0.925 | 0.040 | 11 | 10233236 | intron variant | T/C | snv | 2.2E-02 | 2 | ||
rs11042561 | 0.925 | 0.040 | 11 | 9941510 | intron variant | C/A | snv | 0.20 | 2 | ||
rs7945309 | 1.000 | 0.040 | 11 | 9920885 | intron variant | C/T | snv | 0.12 | 1 | ||
rs11042549 | 1.000 | 0.040 | 11 | 9927031 | intron variant | A/G;T | snv | 1 | |||
rs11042543 | 1.000 | 0.040 | 11 | 9918271 | intron variant | A/G | snv | 0.20 | 1 | ||
rs7102482 | 1.000 | 0.040 | 11 | 9923277 | intron variant | C/T | snv | 0.30 | 1 | ||
rs4910083 | 1.000 | 0.040 | 11 | 9926557 | intron variant | T/C | snv | 0.52 | 1 | ||
rs4450168 | 0.790 | 0.080 | 11 | 10265208 | intron variant | A/C;T | snv | 0.12 | 9 | ||
rs10734650 | 0.925 | 0.080 | 11 | 9820944 | intron variant | C/T | snv | 0.83 | 2 |