Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2078543 | 6 | 21996631 | intron variant | A/G | snv | 0.69 | 1 | ||||
rs4712652 | 1.000 | 0.080 | 6 | 22078386 | intron variant | G/A | snv | 0.64 | 1 | ||
rs6939340 | 0.851 | 0.160 | 6 | 22139775 | intron variant | A/G | snv | 0.62 | 1 | ||
rs7760082 | 6 | 21919156 | intron variant | G/A | snv | 0.59 | 1 | ||||
rs9295536 | 0.882 | 0.080 | 6 | 22131700 | intron variant | C/A | snv | 0.58 | 1 | ||
rs1928175 | 6 | 22079256 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs12212674 | 1.000 | 0.040 | 6 | 22086845 | intron variant | T/A | snv | 0.48 | 1 | ||
rs12196123 | 1.000 | 0.040 | 6 | 22082034 | intron variant | C/T | snv | 0.47 | 1 | ||
rs1205896 | 6 | 22341240 | intron variant | G/A | snv | 0.47 | 1 | ||||
rs1928168 | 6 | 22017509 | intron variant | T/C | snv | 0.36 | 1 | ||||
rs6909752 | 1.000 | 0.040 | 6 | 22612400 | intron variant | G/A | snv | 0.35 | 1 | ||
rs13198081 | 6 | 22017314 | intron variant | G/C | snv | 0.35 | 1 | ||||
rs12525417 | 6 | 22591478 | intron variant | C/T | snv | 0.33 | 1 | ||||
rs6934973 | 6 | 21920795 | intron variant | A/G | snv | 0.32 | 1 | ||||
rs6903716 | 6 | 21956173 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs7766436 | 1.000 | 0.040 | 6 | 22598030 | intron variant | C/T | snv | 0.29 | 1 | ||
rs9466161 | 6 | 21722685 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs6926491 | 6 | 21724439 | intron variant | G/A | snv | 0.21 | 1 | ||||
rs2744132 | 6 | 22392594 | intron variant | G/A | snv | 0.14 | 1 | ||||
rs112204664 | 6 | 21867474 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs9393294 | 6 | 22465392 | intron variant | C/T | snv | 0.13 | 1 | ||||
rs74360995 | 6 | 21886258 | non coding transcript exon variant | T/C | snv | 0.12 | 1 | ||||
rs2479808 | 1.000 | 0.080 | 6 | 21824163 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
rs10484389 | 6 | 22075033 | intron variant | C/T | snv | 6.0E-02 | 1 | ||||
rs113977268 | 6 | 22359286 | intron variant | G/A | snv | 5.7E-02 | 2 |