Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs551517 | 9 | 110874513 | 3 prime UTR variant | C/T | snv | 0.27 | 2 | ||||
rs55905691 | 5 | 111090287 | intron variant | A/G | snv | 0.13 | 2 | ||||
rs79881201 | 5 | 111092097 | 5 prime UTR variant | C/T | snv | 0.26 | 2 | ||||
rs17484848 | 2 | 111142983 | intron variant | T/C | snv | 7.2E-02 | 2 | ||||
rs12935413 | 1.000 | 0.080 | 16 | 11116590 | intron variant | G/A | snv | 0.34 | 3 | ||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs4848100 | 2 | 111630955 | non coding transcript exon variant | C/T | snv | 0.76 | 2 | ||||
rs6803848 | 3 | 112138722 | downstream gene variant | G/A | snv | 5.0E-02 | 2 | ||||
rs555346412 | 12 | 112191863 | intron variant | G/C | snv | 8.2E-04 | 5 | ||||
rs8046011 | 1.000 | 0.120 | 16 | 11226805 | downstream gene variant | G/A;T | snv | 3 | |||
rs62264129 | 3 | 112352566 | intron variant | A/T | snv | 0.27 | 2 | ||||
rs1032726 | 3 | 112967228 | intron variant | T/C | snv | 0.46 | 2 | ||||
rs2029582 | 2 | 113106194 | upstream gene variant | T/C | snv | 0.56 | 4 | ||||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs2846630 | 11 | 114086475 | intron variant | G/A | snv | 0.35 | 5 | ||||
rs238914 | 11 | 114113387 | intron variant | C/A | snv | 0.45 | 5 | ||||
rs3181348 | 9 | 114931904 | intron variant | G/A;C | snv | 2 | |||||
rs66505542 | 11 | 116752498 | intron variant | AA/-;A;AAA | delins | 5 | |||||
rs77204473 | 11 | 116934348 | intron variant | T/C;G | snv | 2 | |||||
rs7008536 | 8 | 118100895 | intron variant | C/A | snv | 0.52 | 1 | ||||
rs143034248 | 11 | 118210555 | missense variant | C/T | snv | 4.0E-03 | 3.5E-03 | 7 |