Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 43 | ||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs55747707 | 7 | 73623036 | intron variant | G/A | snv | 0.16 | 5 | ||||
rs72959041 | 6 | 127133748 | intron variant | G/A | snv | 3.2E-02 | 5 | ||||
rs10049088 | 3 | 157079859 | upstream gene variant | C/T | snv | 0.35 | 3 | ||||
rs11216183 | 11 | 116910829 | intron variant | C/A | snv | 0.10 | 3 | ||||
rs12437696 | 15 | 40586276 | upstream gene variant | A/G | snv | 0.51 | 3 | ||||
rs2306589 | 17 | 36493030 | non coding transcript exon variant | T/C | snv | 0.49 | 3 |