Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4954218 | 0.925 | 0.080 | 2 | 135045855 | intron variant | G/T | snv | 0.83 | 5 | ||
rs6445055 | 0.925 | 0.040 | 3 | 172274597 | intron variant | G/A | snv | 0.24 | 4 | ||
rs9938149 | 0.925 | 0.160 | 16 | 88298034 | intron variant | C/A | snv | 0.66 | 4 | ||
rs10453441 | 1.000 | 0.040 | 22 | 45967859 | intron variant | A/G | snv | 0.40 | 3 | ||
rs12447690 | 1.000 | 0.160 | 16 | 88264518 | intron variant | C/T | snv | 0.53 | 3 | ||
rs2721051 | 1.000 | 0.040 | 13 | 40536747 | intron variant | C/T | snv | 8.6E-02 | 3 | ||
rs7677751 | 0.925 | 0.040 | 4 | 54258293 | intron variant | C/T | snv | 0.18 | 3 | ||
rs11616662 | 13 | 40545329 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs12448211 | 16 | 88296907 | intron variant | G/A | snv | 0.56 | 2 | ||||
rs12913547 | 15 | 67175169 | intron variant | T/C;G | snv | 2 | |||||
rs1324183 | 1.000 | 0.040 | 9 | 13557492 | intron variant | A/C;T | snv | 2 | |||
rs2114039 | 1.000 | 0.080 | 4 | 54226459 | intron variant | T/C | snv | 0.40 | 2 | ||
rs2755237 | 13 | 40535292 | intron variant | A/C | snv | 0.17 | 2 | ||||
rs3931397 | 1.000 | 0.080 | 4 | 148158346 | intron variant | G/T | snv | 0.11 | 2 | ||
rs4894535 | 1.000 | 0.040 | 3 | 172277815 | intron variant | C/A;T | snv | 2 | |||
rs4948502 | 1.000 | 0.040 | 10 | 62079658 | intron variant | T/C | snv | 0.33 | 2 | ||
rs6430585 | 1.000 | 0.040 | 2 | 135749357 | intron variant | A/C | snv | 0.74 | 2 | ||
rs6540223 | 16 | 88287830 | intron variant | C/T | snv | 0.72 | 2 | ||||
rs7044529 | 1.000 | 0.040 | 9 | 134676205 | intron variant | C/T | snv | 0.21 | 2 | ||
rs752092 | 15 | 101241729 | intron variant | A/G | snv | 0.43 | 2 | ||||
rs7606754 | 1.000 | 0.040 | 2 | 227270464 | intron variant | A/G | snv | 0.69 | 2 | ||
rs785422 | 15 | 29881682 | intron variant | C/T | snv | 1.0E-01 | 2 | ||||
rs930847 | 15 | 101018357 | intron variant | G/T | snv | 0.67 | 2 | ||||
rs96067 | 1 | 36106319 | intron variant | G/A | snv | 0.73 | 2 | ||||
rs9822953 | 3 | 156754282 | intron variant | C/G;T | snv | 2 |