Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs757608 | 17 | 61419916 | regulatory region variant | A/G;T | snv | 4 | |||||
rs7697556 | 4 | 72649596 | intergenic variant | T/A;C | snv | 4 | |||||
rs7763064 | 6 | 142476152 | intergenic variant | G/A | snv | 0.38 | 4 | ||||
rs11750568 | 1.000 | 0.080 | 5 | 179108712 | downstream gene variant | A/G;T | snv | 3 | |||
rs117642368 | 17 | 45321692 | upstream gene variant | G/C | snv | 6.9E-02 | 3 | ||||
rs1582931 | 5 | 123321505 | intergenic variant | G/A;T | snv | 3 | |||||
rs1659127 | 16 | 14294448 | intergenic variant | G/A;C;T | snv | 3 | |||||
rs1759645 | 6 | 34227089 | TF binding site variant | C/T | snv | 0.71 | 3 | ||||
rs2079795 | 17 | 61419288 | regulatory region variant | T/A;C | snv | 3 | |||||
rs2597513 | 1.000 | 0.040 | 3 | 13514336 | regulatory region variant | C/T | snv | 0.88 | 3 | ||
rs2731880 | 0.925 | 0.040 | 5 | 36603282 | upstream gene variant | T/C | snv | 0.52 | 3 | ||
rs2778031 | 1.000 | 0.040 | 9 | 88220811 | intergenic variant | T/A;C | snv | 3 | |||
rs2780226 | 6 | 34231315 | regulatory region variant | C/T | snv | 0.80 | 3 | ||||
rs28600726 | 1.000 | 0.040 | 4 | 158730723 | intergenic variant | G/A | snv | 0.53 | 3 | ||
rs4549631 | 6 | 126645162 | intron variant | T/C;G | snv | 3 | |||||
rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 3 | ||||
rs4794665 | 1.000 | 0.160 | 17 | 56772968 | intergenic variant | A/C;G | snv | 3 | |||
rs6449353 | 4 | 18031865 | intergenic variant | T/C | snv | 0.26 | 3 | ||||
rs710841 | 4 | 81228677 | intergenic variant | C/T | snv | 0.37 | 3 | ||||
rs7534091 | 1 | 118321993 | intergenic variant | A/G | snv | 0.23 | 3 | ||||
rs7713145 | 1.000 | 0.040 | 5 | 177354208 | upstream gene variant | G/A | snv | 0.37 | 3 | ||
rs7742369 | 6 | 34197944 | TF binding site variant | A/G | snv | 0.30 | 3 | ||||
rs7846385 | 8 | 77247943 | intergenic variant | T/C | snv | 0.23 | 3 | ||||
rs7968682 | 12 | 65978100 | intergenic variant | G/T | snv | 0.56 | 3 | ||||
rs8099594 | 1.000 | 0.040 | 18 | 49464790 | upstream gene variant | A/C;G;T | snv | 3 |