Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74360995 | 6 | 21886258 | non coding transcript exon variant | T/C | snv | 0.12 | 1 | ||||
rs1205896 | 6 | 22341240 | intron variant | G/A | snv | 0.47 | 1 | ||||
rs9393294 | 6 | 22465392 | intron variant | C/T | snv | 0.13 | 1 | ||||
rs12525417 | 6 | 22591478 | intron variant | C/T | snv | 0.33 | 1 | ||||
rs196052 | 1.000 | 0.040 | 6 | 22056971 | intron variant | T/A;C | snv | 1 | |||
rs9350395 | 1.000 | 0.080 | 6 | 21905495 | intron variant | A/G;T | snv | 1 | |||
rs2744133 | 6 | 22392031 | intron variant | A/G;T | snv | 1 | |||||
rs6911827 | 6 | 22130372 | intron variant | C/G;T | snv | 1 | |||||
rs9466161 | 6 | 21722685 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs7760082 | 6 | 21919156 | intron variant | G/A | snv | 0.59 | 1 | ||||
rs6934973 | 6 | 21920795 | intron variant | A/G | snv | 0.32 | 1 | ||||
rs13198081 | 6 | 22017314 | intron variant | G/C | snv | 0.35 | 1 | ||||
rs7766436 | 1.000 | 0.040 | 6 | 22598030 | intron variant | C/T | snv | 0.29 | 1 | ||
rs6909752 | 1.000 | 0.040 | 6 | 22612400 | intron variant | G/A | snv | 0.35 | 1 | ||
rs2876643 | 1.000 | 0.040 | 6 | 22591296 | intron variant | C/A;T | snv | 1 | |||
rs141007801 | 6 | 21722558 | intron variant | A/-;AA;AAA;AAAA | delins | 2 |