Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2294214 | 0.882 | 0.040 | 6 | 22056694 | splice region variant | A/C;T | snv | 6 | |||
rs4712656 | 1.000 | 0.040 | 6 | 22136033 | non coding transcript exon variant | G/A;C | snv | 4 | |||
rs55775505 | 0.882 | 0.040 | 6 | 22057337 | intron variant | C/A;G;T | snv | 3 | |||
rs113760175 | 6 | 22343363 | intron variant | G/A;T | snv | 3 | |||||
rs141007801 | 6 | 21722558 | intron variant | A/-;AA;AAA;AAAA | delins | 2 | |||||
rs113977268 | 6 | 22359286 | intron variant | G/A | snv | 5.7E-02 | 2 | ||||
rs2479808 | 1.000 | 0.080 | 6 | 21824163 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
rs12196123 | 1.000 | 0.040 | 6 | 22082034 | intron variant | C/T | snv | 0.47 | 1 | ||
rs12212674 | 1.000 | 0.040 | 6 | 22086845 | intron variant | T/A | snv | 0.48 | 1 | ||
rs10946507 | 1.000 | 0.040 | 6 | 22100138 | intron variant | G/A;T | snv | 1 | |||
rs6926491 | 6 | 21724439 | intron variant | G/A | snv | 0.21 | 1 | ||||
rs10484389 | 6 | 22075033 | intron variant | C/T | snv | 6.0E-02 | 1 | ||||
rs67258057 | 6 | 21948833 | intron variant | G/A | snv | 4.8E-02 | 1 | ||||
rs6903716 | 6 | 21956173 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs7763264 | 6 | 21959834 | intron variant | C/G;T | snv | 1 | |||||
rs1928175 | 6 | 22079256 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs13198656 | 1.000 | 0.040 | 6 | 22004680 | intron variant | C/A;T | snv | 1 | |||
rs9295536 | 0.882 | 0.080 | 6 | 22131700 | intron variant | C/A | snv | 0.58 | 1 | ||
rs4712653 | 0.882 | 0.080 | 6 | 22125735 | intron variant | T/C;G | snv | 1 | |||
rs4712652 | 1.000 | 0.080 | 6 | 22078386 | intron variant | G/A | snv | 0.64 | 1 | ||
rs3736675 | 6 | 22110919 | splice region variant | G/A | snv | 3.0E-02 | 1 | ||||
rs1928168 | 6 | 22017509 | intron variant | T/C | snv | 0.36 | 1 | ||||
rs2078543 | 6 | 21996631 | intron variant | A/G | snv | 0.69 | 1 | ||||
rs112204664 | 6 | 21867474 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs74360995 | 6 | 21886258 | non coding transcript exon variant | T/C | snv | 0.12 | 1 |