Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 3 | |
rs2858829 | 1.000 | 0.040 | 6 | 116447754 | intron variant | A/G | snv | 0.33 | 2 | ||
rs2637678 | 6 | 116466215 | upstream gene variant | T/C | snv | 0.36 | 1 | ||||
rs2858317 | 6 | 32694503 | intergenic variant | C/A | snv | 0.41 | 1 | ||||
rs4642516 | 6 | 32689766 | TF binding site variant | G/A;T | snv | 1 | |||||
rs2746419 | 6 | 135332717 | intron variant | A/C | snv | 0.46 | 1 | ||||
rs59882675 | 4 | 74763902 | intron variant | A/G | snv | 0.23 | 1 | ||||
rs16946160 | 13 | 91551559 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs1063348 | 1.000 | 0.080 | 6 | 32660146 | 3 prime UTR variant | A/G | snv | 0.43 | 1 | ||
rs9273542 | 6 | 32661035 | intron variant | C/A;T | snv | 1 | |||||
rs28366266 | 6 | 32591976 | upstream gene variant | T/C | snv | 0.12 | 1 | ||||
rs487575 | 3 | 187880609 | intergenic variant | C/T | snv | 0.23 | 1 | ||||
rs10518133 | 4 | 75025495 | intron variant | G/A | snv | 9.7E-02 | 1 | ||||
rs201899638 | 9 | 9932324 | intron variant | T/C;G | snv | 1 | |||||
rs9348883 | 6 | 32390772 | non coding transcript exon variant | T/A;G | snv | 1 |