Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs174536 | 11 | 61784455 | non coding transcript exon variant | A/C | snv | 0.29 | 3 | ||||
rs174574 | 1.000 | 0.080 | 11 | 61832870 | intron variant | A/C | snv | 0.55 | 7 | ||
rs7394871 | 11 | 61885042 | intron variant | A/C;T | snv | 2 | |||||
rs1000778 | 1.000 | 0.040 | 11 | 61887833 | intron variant | A/G | snv | 0.59 | 3 | ||
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 12 | ||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 24 | ||
rs174464 | 11 | 61890454 | intron variant | A/G | snv | 0.59 | 2 | ||||
rs174472 | 11 | 61904484 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs174534 | 1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 | 3 | ||
rs2072114 | 1.000 | 0.080 | 11 | 61837743 | intron variant | A/G | snv | 0.19 | 0.16 | 4 | |
rs2727266 | 11 | 61936862 | upstream gene variant | A/G | snv | 9.8E-02 | 2 | ||||
rs2845573 | 1.000 | 0.040 | 11 | 61834436 | intron variant | A/G | snv | 9.7E-02 | 3 | ||
rs2851682 | 11 | 61848540 | intron variant | A/G | snv | 9.9E-02 | 5 | ||||
rs509360 | 11 | 61781087 | intron variant | A/G | snv | 0.61 | 0.52 | 3 | |||
rs7200543 | 16 | 15036113 | synonymous variant | A/G | snv | 0.35 | 0.30 | 6 | |||
rs17156426 | 11 | 61841851 | intron variant | A/G;T | snv | 2 | |||||
rs4453795 | 3 | 192376186 | intron variant | A/G;T | snv | 2 | |||||
rs10517480 | 4 | 59883111 | intergenic variant | A/T | snv | 0.27 | 2 | ||||
rs2524299 | 11 | 61837310 | intron variant | A/T | snv | 0.17 | 2 | ||||
rs2727271 | 11 | 61835886 | intron variant | A/T | snv | 0.12 | 2 | ||||
rs1109748 | 11 | 61955173 | synonymous variant | C/A | snv | 0.21 | 0.11 | 2 | |||
rs174456 | 11 | 61888710 | intron variant | C/A | snv | 0.59 | 2 | ||||
rs174476 | 11 | 61906646 | synonymous variant | C/A;G;T | snv | 0.30 | 2 | ||||
rs174479 | 11 | 61911282 | intron variant | C/G | snv | 0.17 | 2 | ||||
rs174575 | 1.000 | 0.040 | 11 | 61834531 | intron variant | C/G | snv | 0.25 | 3 |