Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1573643 | 15 | 90877743 | intron variant | T/C | snv | 0.33 | 5 | ||||
rs17035646 | 1 | 10736490 | intron variant | G/A;T | snv | 6 | |||||
rs17249754 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 12 | ||
rs1731249 | 2 | 26697157 | intron variant | T/A | snv | 0.48 | 5 | ||||
rs17367504 | 1.000 | 0.040 | 1 | 11802721 | intron variant | A/G | snv | 0.14 | 9 | ||
rs1813353 | 10 | 18418519 | intron variant | T/C | snv | 0.29 | 5 | ||||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 10 | |||
rs2932538 | 1 | 112673921 | intron variant | A/C;G | snv | 4 | |||||
rs381815 | 1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 | 6 | ||
rs419076 | 3 | 169383098 | intron variant | T/A;C | snv | 6 | |||||
rs438885 | 2 | 164195781 | intron variant | A/T | snv | 0.56 | 5 | ||||
rs4590817 | 10 | 61707795 | intron variant | G/C | snv | 0.15 | 5 | ||||
rs5883070 | 7 | 27240226 | intron variant | -/AAAACA;AACA | delins | 0.91 | 5 | ||||
rs6015450 | 20 | 59176062 | intron variant | A/G | snv | 0.14 | 7 | ||||
rs62434109 | 6 | 150654176 | intron variant | T/G | snv | 8.4E-02 | 5 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs7129220 | 11 | 10328991 | intron variant | G/A | snv | 0.10 | 5 | ||||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs805303 | 0.925 | 0.160 | 6 | 31648589 | intron variant | G/A | snv | 0.45 | 7 | ||
rs932764 | 10 | 94136183 | intron variant | A/G | snv | 0.38 | 6 |