Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17596143 | 11 | 55910869 | downstream gene variant | T/A | snv | 5.7E-02 | 1 | ||||
rs17597169 | 11 | 55921634 | intergenic variant | T/C | snv | 5.8E-02 | 1 | ||||
rs17597302 | 11 | 55922387 | intergenic variant | C/T | snv | 5.8E-02 | 1 | ||||
rs17598045 | 11 | 55940815 | upstream gene variant | G/A;T | snv | 1 | |||||
rs17598094 | 11 | 55941339 | upstream gene variant | T/C | snv | 6.0E-02 | 1 | ||||
rs17599471 | 11 | 55959133 | upstream gene variant | G/A | snv | 6.1E-02 | 1 | ||||
rs17602278 | 11 | 56081639 | upstream gene variant | T/C | snv | 6.0E-02 | 1 | ||||
rs17603373 | 11 | 56118743 | upstream gene variant | T/C | snv | 5.8E-02 | 1 | ||||
rs17610514 | 11 | 56128322 | downstream gene variant | A/G | snv | 6.0E-02 | 1 | ||||
rs1876924 | 11 | 56580160 | upstream gene variant | G/A | snv | 5.9E-02 | 1 | ||||
rs1957563 | 5 | 158047582 | intergenic variant | C/T | snv | 0.25 | 1 | ||||
rs2145067 | 6 | 94547045 | intergenic variant | C/T | snv | 0.16 | 1 | ||||
rs2702888 | 8 | 6907510 | intergenic variant | G/A;C;T | snv | 1 | |||||
rs2969070 | 7 | 2472910 | downstream gene variant | G/A;C | snv | 1 | |||||
rs35444 | 12 | 115114632 | intergenic variant | A/G | snv | 0.38 | 1 | ||||
rs4141856 | 19 | 50865248 | intron variant | C/T | snv | 0.61 | 1 | ||||
rs4638749 | 2 | 108267586 | downstream gene variant | G/A | snv | 0.26 | 1 | ||||
rs4685307 | 3 | 16123911 | regulatory region variant | G/A;T | snv | 1 | |||||
rs4842666 | 12 | 89547772 | non coding transcript exon variant | T/C | snv | 0.16 | 1 | ||||
rs4977950 | 9 | 24732484 | intergenic variant | G/C;T | snv | 1 | |||||
rs6763470 | 3 | 55390915 | intergenic variant | T/A;G | snv | 1 | |||||
rs6892243 | 5 | 104843088 | intron variant | G/A | snv | 9.0E-02 | 1 | ||||
rs7088591 | 10 | 57964643 | regulatory region variant | A/T | snv | 9.3E-02 | 1 | ||||
rs7108801 | 11 | 56309124 | intergenic variant | C/T | snv | 5.9E-02 | 1 | ||||
rs7110667 | 11 | 34006534 | regulatory region variant | A/T | snv | 0.22 | 1 |