Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1040552 | 20 | 33861523 | regulatory region variant | A/G | snv | 0.19 | 2 | ||||
rs12465955 | 2 | 127249498 | non coding transcript exon variant | A/G;T | snv | 2 | |||||
rs12625191 | 20 | 35623371 | downstream gene variant | C/G | snv | 6.7E-02 | 2 | ||||
rs13037376 | 20 | 35297352 | upstream gene variant | T/C | snv | 0.35 | 2 | ||||
rs13038810 | 20 | 36282301 | intergenic variant | A/C;G | snv | 2 | |||||
rs13041173 | 20 | 33955008 | intergenic variant | A/G | snv | 0.25 | 2 | ||||
rs148639156 | 6 | 39144635 | intergenic variant | A/G | snv | 3.1E-03 | 2 | ||||
rs1566822 | 2 | 127229815 | intergenic variant | A/G | snv | 0.40 | 2 | ||||
rs1604817 | 2 | 127242345 | upstream gene variant | C/T | snv | 0.61 | 2 | ||||
rs17302686 | 20 | 34322499 | TF binding site variant | G/A | snv | 4.0E-02 | 2 | ||||
rs17332951 | 20 | 34176377 | regulatory region variant | T/C | snv | 3.6E-02 | 2 | ||||
rs2092477 | 20 | 33896623 | regulatory region variant | T/A;C | snv | 2 | |||||
rs2174270 | 2 | 127248502 | non coding transcript exon variant | C/G;T | snv | 2 | |||||
rs224320 | 20 | 35422754 | intergenic variant | G/A | snv | 0.88 | 2 | ||||
rs2425207 | 20 | 36271121 | downstream gene variant | G/A | snv | 7.9E-02 | 2 | ||||
rs2425215 | 20 | 36282083 | intergenic variant | T/G | snv | 0.12 | 2 | ||||
rs2425219 | 20 | 36286427 | intergenic variant | C/A;T | snv | 2 | |||||
rs3761135 | 20 | 35744478 | upstream gene variant | C/T | snv | 7.0E-02 | 2 | ||||
rs42238 | 7 | 73416216 | intergenic variant | C/G;T | snv | 2 | |||||
rs4324393 | 20 | 33949027 | intergenic variant | G/A;C | snv | 2 | |||||
rs4510165 | 2 | 127178708 | intergenic variant | C/T | snv | 0.10 | 2 | ||||
rs4536600 | 2 | 127244996 | upstream gene variant | G/A | snv | 0.59 | 2 | ||||
rs4662713 | 2 | 127236527 | intergenic variant | C/A;T | snv | 2 | |||||
rs4662717 | 2 | 127255928 | downstream gene variant | C/T | snv | 0.47 | 2 | ||||
rs4663109 | 2 | 127164716 | intergenic variant | A/G | snv | 0.78 | 2 |