Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs110420 | 0.882 | 0.080 | 11 | 8231502 | intron variant | T/C | snv | 0.42 | 3 | ||
rs12442054 | 0.882 | 0.080 | 15 | 74165683 | intron variant | G/A | snv | 0.12 | 3 | ||
rs17065417 | 0.882 | 0.080 | 6 | 104958399 | intron variant | A/C | snv | 0.10 | 3 | ||
rs17251 | 0.925 | 0.120 | 7 | 142715462 | intron variant | C/A | snv | 0.33 | 0.37 | 3 | |
rs17487792 | 0.882 | 0.080 | 2 | 214778776 | intron variant | C/T | snv | 0.16 | 3 | ||
rs204926 | 0.882 | 0.080 | 11 | 8233559 | intron variant | G/A | snv | 0.41 | 3 | ||
rs204938 | 0.882 | 0.080 | 11 | 8256650 | intron variant | C/T | snv | 0.49 | 3 | ||
rs2302616 | 0.882 | 0.080 | 2 | 10448065 | intron variant | C/A | snv | 0.26 | 3 | ||
rs2619046 | 0.882 | 0.080 | 5 | 55801706 | intron variant | G/A | snv | 0.34 | 3 | ||
rs3768707 | 0.882 | 0.080 | 2 | 214780411 | intron variant | A/G | snv | 0.74 | 3 | ||
rs3796725 | 0.882 | 0.080 | 4 | 8616210 | intron variant | C/T | snv | 0.23 | 3 | ||
rs3796727 | 0.882 | 0.080 | 4 | 8611299 | intron variant | G/A | snv | 0.26 | 0.32 | 3 | |
rs4712653 | 0.882 | 0.080 | 6 | 22125735 | intron variant | T/C;G | snv | 3 | |||
rs6441201 | 0.882 | 0.080 | 3 | 158460535 | intron variant | G/A | snv | 0.51 | 3 | ||
rs80059929 | 0.882 | 0.080 | 3 | 44805230 | intron variant | T/A | snv | 3.6E-02 | 3 | ||
rs9295536 | 0.882 | 0.080 | 6 | 22131700 | intron variant | C/A | snv | 0.58 | 3 | ||
rs9404576 | 0.882 | 0.160 | 6 | 104736765 | intron variant | T/A;G | snv | 3 | |||
rs9653226 | 0.882 | 0.080 | 2 | 15939632 | intron variant | C/T | snv | 0.54 | 3 | ||
rs10131293 | 1.000 | 0.040 | 14 | 22461166 | intron variant | G/A | snv | 0.15 | 1 | ||
rs10132733 | 1.000 | 0.040 | 14 | 22477241 | intron variant | A/G | snv | 0.19 | 1 | ||
rs10142552 | 1.000 | 0.040 | 14 | 22395232 | intron variant | G/A | snv | 3.5E-02 | 1 | ||
rs10148895 | 1.000 | 0.040 | 14 | 22254840 | intron variant | C/T | snv | 0.18 | 1 | ||
rs10162417 | 1.000 | 0.040 | 14 | 22460708 | intron variant | T/G | snv | 0.15 | 1 | ||
rs1040303 | 1.000 | 0.040 | 14 | 22403377 | intron variant | G/A | snv | 0.13 | 1 | ||
rs10483273 | 1.000 | 0.040 | 14 | 22448054 | intron variant | A/G | snv | 9.5E-02 | 1 |