Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10747083 | 12 | 132465032 | downstream gene variant | G/A;T | snv | 2 | |||||
rs11039130 | 11 | 47207765 | intergenic variant | C/T | snv | 0.20 | 2 | ||||
rs11195502 | 10 | 111279909 | intergenic variant | C/A;G;T | snv | 2 | |||||
rs11607883 | 11 | 45818158 | intron variant | G/A | snv | 0.40 | 2 | ||||
rs11782386 | 8 | 9344277 | intron variant | C/T | snv | 9.7E-02 | 2 | ||||
rs118137427 | 10 | 111217250 | intergenic variant | A/G | snv | 3.3E-02 | 2 | ||||
rs1280 | 3 | 170995501 | intron variant | T/C | snv | 0.20 | 2 | ||||
rs4775471 | 15 | 62132450 | intergenic variant | C/T | snv | 0.18 | 2 | ||||
rs983309 | 8 | 9320222 | intron variant | T/G | snv | 0.82 | 2 | ||||
rs11715915 | 3 | 49417897 | synonymous variant | C/A;T | snv | 0.28 | 2 | ||||
rs7101470 | 11 | 47032897 | intron variant | A/G | snv | 7.4E-02 | 2 | ||||
rs3829109 | 9 | 136362314 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs2390732 | 2 | 168749457 | intron variant | G/A | snv | 0.65 | 2 | ||||
rs16913693 | 9 | 108918079 | intron variant | T/G | snv | 8.4E-02 | 2 | ||||
rs8020333 | 14 | 89568505 | intron variant | C/G;T | snv | 0.52 | 2 | ||||
rs2268575 | 7 | 44149675 | intron variant | T/C | snv | 0.18 | 2 | ||||
rs4237150 | 9 | 4290085 | intron variant | G/A;C;T | snv | 2 | |||||
rs7867224 | 9 | 4292152 | intron variant | A/C;G | snv | 0.37 | 2 | ||||
rs2300615 | 6 | 39071727 | intron variant | T/G | snv | 0.17 | 2 | ||||
rs6943153 | 7 | 50723882 | intron variant | T/C | snv | 0.56 | 2 | ||||
rs1983127 | 10 | 69230145 | intron variant | G/T | snv | 0.38 | 2 | ||||
rs2280231 | 11 | 47578886 | 5 prime UTR variant | C/T | snv | 0.24 | 0.20 | 2 | |||
rs6113722 | 20 | 22576461 | intron variant | G/A;T | snv | 2 | |||||
rs2971671 | 7 | 44171738 | intron variant | T/C | snv | 0.22 | 2 | ||||
rs35859536 | 8 | 117179236 | downstream gene variant | C/T | snv | 0.25 | 2 |