Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10484389 | 6 | 22075033 | intron variant | C/T | snv | 6.0E-02 | 1 | ||||
rs10946507 | 1.000 | 0.040 | 6 | 22100138 | intron variant | G/A;T | snv | 1 | |||
rs112204664 | 6 | 21867474 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs113760175 | 6 | 22343363 | intron variant | G/A;T | snv | 3 | |||||
rs113977268 | 6 | 22359286 | intron variant | G/A | snv | 5.7E-02 | 2 | ||||
rs1205896 | 6 | 22341240 | intron variant | G/A | snv | 0.47 | 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 | ||
rs12525417 | 6 | 22591478 | intron variant | C/T | snv | 0.33 | 1 | ||||
rs13198081 | 6 | 22017314 | intron variant | G/C | snv | 0.35 | 1 | ||||
rs13198656 | 1.000 | 0.040 | 6 | 22004680 | intron variant | C/A;T | snv | 1 | |||
rs141007801 | 6 | 21722558 | intron variant | A/-;AA;AAA;AAAA | delins | 2 | |||||
rs1928168 | 6 | 22017509 | intron variant | T/C | snv | 0.36 | 1 | ||||
rs1928175 | 6 | 22079256 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs196052 | 1.000 | 0.040 | 6 | 22056971 | intron variant | T/A;C | snv | 1 | |||
rs2078543 | 6 | 21996631 | intron variant | A/G | snv | 0.69 | 1 | ||||
rs2294214 | 0.882 | 0.040 | 6 | 22056694 | splice region variant | A/C;T | snv | 6 | |||
rs2479808 | 1.000 | 0.080 | 6 | 21824163 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
rs2744132 | 6 | 22392594 | intron variant | G/A | snv | 0.14 | 1 | ||||
rs2744133 | 6 | 22392031 | intron variant | A/G;T | snv | 1 | |||||
rs2876643 | 1.000 | 0.040 | 6 | 22591296 | intron variant | C/A;T | snv | 1 | |||
rs3736675 | 6 | 22110919 | splice region variant | G/A | snv | 3.0E-02 | 1 | ||||
rs4712652 | 1.000 | 0.080 | 6 | 22078386 | intron variant | G/A | snv | 0.64 | 1 | ||
rs4712653 | 0.882 | 0.080 | 6 | 22125735 | intron variant | T/C;G | snv | 1 | |||
rs4712656 | 1.000 | 0.040 | 6 | 22136033 | non coding transcript exon variant | G/A;C | snv | 4 |