Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | ||||
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 | ||||
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 | ||||
rs4813376 | 20 | 19870811 | intron variant | T/G | snv | 0.86 | 2 | ||||
rs4996815 | 13 | 105999312 | intron variant | G/T | snv | 0.61 | 2 | ||||
rs6024905 | 20 | 38329435 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs6046396 | 20 | 19871859 | non coding transcript exon variant | G/A | snv | 0.68 | 2 | ||||
rs6444931 | 3 | 170445686 | intron variant | G/A | snv | 0.85 | 2 | ||||
rs6627057 | X | 145059799 | downstream gene variant | T/G | snv | 0.16 | 2 |