Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12549576 | 8 | 111963912 | intergenic variant | A/G | snv | 4.0E-02 | 2 | ||||
rs2266887 | X | 153974136 | intron variant | G/C;T | snv | 2 | |||||
rs5987245 | X | 154323037 | intron variant | A/G | snv | 0.22 | 2 | ||||
rs766420 | X | 154326058 | intron variant | C/G | snv | 0.32 | 2 | ||||
rs766419 | X | 154326315 | intron variant | A/G | snv | 0.31 | 2 | ||||
rs2239467 | X | 154326948 | intron variant | A/G | snv | 0.28 | 2 | ||||
rs2239468 | X | 154327040 | intron variant | T/A | snv | 0.36 | 2 | ||||
rs12823467 | 12 | 20790642 | intergenic variant | T/C | snv | 0.59 | 2 | ||||
rs12313384 | 12 | 20790827 | intergenic variant | G/T | snv | 0.58 | 2 | ||||
rs10841642 | 12 | 20791740 | intergenic variant | C/A;T | snv | 2 | |||||
rs4762785 | 12 | 20792339 | intergenic variant | T/A;G | snv | 2 | |||||
rs10841645 | 12 | 20795800 | intergenic variant | A/C | snv | 0.59 | 2 | ||||
rs11045505 | 12 | 20796512 | intergenic variant | C/T | snv | 0.59 | 2 | ||||
rs10841648 | 12 | 20801623 | intergenic variant | C/A;T | snv | 2 | |||||
rs2417940 | 12 | 20864941 | intron variant | T/A;C | snv | 3 | |||||
rs11045598 | 12 | 20918279 | intron variant | A/G | snv | 0.14 | 2 | ||||
rs2117032 | 12 | 20921188 | intron variant | C/T | snv | 0.47 | 2 | ||||
rs12366506 | 12 | 20926661 | intron variant | C/T | snv | 0.14 | 2 | ||||
rs11045603 | 12 | 20930460 | intron variant | A/G;T | snv | 2 | |||||
rs10841712 | 12 | 20933449 | intron variant | A/G | snv | 0.47 | 2 | ||||
rs11045611 | 12 | 20946338 | intron variant | A/C | snv | 0.14 | 2 | ||||
rs1910196 | 12 | 20964279 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs11045626 | 12 | 20965963 | intron variant | A/G | snv | 0.14 | 2 | ||||
rs11045627 | 12 | 20966129 | intron variant | C/G;T | snv | 2 | |||||
rs11045630 | 12 | 20972587 | intron variant | T/C | snv | 0.14 | 2 |