Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 7 | ||||
rs9983925 | 21 | 45216929 | intron variant | C/T | snv | 0.46 | 4 | ||||
rs4675690 | 2 | 207643083 | intergenic variant | C/T | snv | 0.48 | 3 | ||||
rs1009080 | 1 | 29958713 | intergenic variant | G/A | snv | 0.54 | 2 | ||||
rs10496702 | 2 | 133247997 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs10949808 | 7 | 156255955 | intergenic variant | T/G | snv | 0.45 | 2 | ||||
rs11164835 | 1 | 92913536 | intron variant | G/A | snv | 0.35 | 2 | ||||
rs11740562 | 5 | 157515277 | intron variant | A/G | snv | 7.1E-02 | 2 | ||||
rs11789407 | 9 | 118597268 | intergenic variant | C/A | snv | 0.44 | 2 | ||||
rs12282742 | 11 | 18244252 | intron variant | C/G;T | snv | 2 | |||||
rs12527359 | 6 | 89018502 | intergenic variant | T/A | snv | 0.23 | 2 | ||||
rs12745968 | 1 | 92936280 | intron variant | A/G | snv | 0.36 | 2 | ||||
rs17069122 | 6 | 108002555 | downstream gene variant | G/A | snv | 1.9E-02 | 2 | ||||
rs17075286 | 3 | 43189231 | intergenic variant | C/G | snv | 5.9E-02 | 2 | ||||
rs1799920 | 5 | 63961656 | missense variant | C/G;T | snv | 3.2E-04 | 2 | ||||
rs1799921 | 5 | 63961638 | missense variant | T/C | snv | 9.4E-03 | 9.3E-03 | 2 | |||
rs1806864 | 9 | 87416754 | regulatory region variant | G/C | snv | 7.4E-02 | 2 | ||||
rs1992044 | 8 | 57928349 | intron variant | G/A;T | snv | 2 | |||||
rs1992045 | 8 | 57928365 | intron variant | C/T | snv | 0.14 | 2 | ||||
rs2018368 | 11 | 10718819 | intergenic variant | C/G | snv | 0.59 | 2 | ||||
rs2044117 | 13 | 101055958 | intron variant | G/A | snv | 0.19 | 2 | ||||
rs2049161 | 18 | 4127583 | intron variant | A/C;T | snv | 0.22 | 2 | ||||
rs2155907 | 11 | 98223945 | intergenic variant | C/T | snv | 0.38 | 2 | ||||
rs2509843 | 11 | 98254676 | intergenic variant | A/C;G;T | snv | 2 | |||||
rs2841307 | 6 | 100308811 | intergenic variant | C/T | snv | 0.20 | 2 |