Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs141424017 | 1.000 | 0.080 | 7 | 115311376 | intergenic variant | -/CAA | ins | 3 | |||
rs1437396 | 1.000 | 0.080 | 2 | 55278320 | upstream gene variant | C/G;T | snv | 3 | |||
rs1660895 | 1.000 | 0.080 | 2 | 129236759 | intergenic variant | A/T | snv | 0.52 | 3 | ||
rs17125651 | 1.000 | 0.080 | 10 | 109063325 | intergenic variant | T/C | snv | 0.14 | 3 | ||
rs2168784 | 1.000 | 0.080 | 3 | 164872151 | intergenic variant | C/T | snv | 0.24 | 3 | ||
rs4699741 | 1.000 | 0.080 | 4 | 99357540 | upstream gene variant | T/C | snv | 9.2E-02 | 3 | ||
rs4715221 | 1.000 | 0.080 | 6 | 51495005 | regulatory region variant | G/A;C;T | snv | 3 | |||
rs4936277 | 1.000 | 0.080 | 11 | 113561238 | intergenic variant | A/G | snv | 0.37 | 3 | ||
rs540606 | 1.000 | 0.080 | 2 | 44911368 | intergenic variant | A/G | snv | 0.66 | 3 | ||
rs570436 | 1.000 | 0.080 | 2 | 44915534 | intergenic variant | C/T | snv | 0.69 | 3 | ||
rs61776290 | 1.000 | 0.080 | 1 | 10634850 | upstream gene variant | C/T | snv | 8.7E-02 | 3 | ||
rs61902812 | 1.000 | 0.080 | 11 | 113503698 | intergenic variant | C/A | snv | 0.26 | 3 | ||
rs6701037 | 1.000 | 0.080 | 1 | 175150943 | downstream gene variant | A/C;T | snv | 3 | |||
rs6777876 | 1.000 | 0.080 | 3 | 11915124 | upstream gene variant | A/G | snv | 9.9E-02 | 3 | ||
rs72716801 | 1.000 | 0.080 | 8 | 127636481 | non coding transcript exon variant | G/T | snv | 5.5E-02 | 3 | ||
rs73135175 | 1.000 | 0.080 | 4 | 45545051 | intergenic variant | C/T | snv | 0.15 | 3 | ||
rs74745534 | 1.000 | 0.080 | 6 | 49589080 | intergenic variant | C/T | snv | 2.1E-02 | 3 | ||
rs7913179 | 1.000 | 0.080 | 10 | 97705109 | intergenic variant | C/A;G;T | snv | 3 | |||
rs9512637 | 1.000 | 0.080 | 13 | 27346474 | upstream gene variant | T/C | snv | 0.55 | 3 | ||
rs1154433 | 1.000 | 0.080 | 4 | 99332551 | intron variant | A/G;T | snv | 3 | |||
rs1693457 | 1.000 | 0.080 | 4 | 99315605 | non coding transcript exon variant | C/T | snv | 0.81 | 3 | ||
rs1789891 | 1.000 | 0.080 | 4 | 99329262 | intron variant | C/A | snv | 0.13 | 3 | ||
rs2066702 | 0.882 | 0.080 | 4 | 99307860 | missense variant | G/A | snv | 1.5E-02 | 5.9E-02 | 3 | |
rs2075633 | 1.000 | 0.080 | 4 | 99317841 | non coding transcript exon variant | T/C | snv | 0.24 | 3 | ||
rs2173201 | 1.000 | 0.080 | 4 | 99329813 | intron variant | C/A | snv | 0.30 | 3 |