Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9834970 | 0.790 | 0.080 | 3 | 36814539 | downstream gene variant | T/C | snv | 0.45 | 9 | ||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 7 | ||||
rs4650608 | 0.851 | 0.040 | 1 | 78772330 | intergenic variant | T/C | snv | 0.29 | 7 | ||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs12201676 | 0.925 | 0.040 | 6 | 89022382 | regulatory region variant | T/C | snv | 0.21 | 4 | ||
rs17746001 | 0.925 | 0.040 | 4 | 179734472 | intergenic variant | C/T | snv | 5.3E-02 | 4 | ||
rs17645023 | 1.000 | 0.040 | 17 | 66920916 | intergenic variant | A/T | snv | 0.22 | 3 | ||
rs4537731 | 1.000 | 0.040 | 11 | 18047335 | upstream gene variant | T/C | snv | 0.48 | 3 | ||
rs4675690 | 2 | 207643083 | intergenic variant | C/T | snv | 0.48 | 3 | ||||
rs4949526 | 1.000 | 0.040 | 1 | 29959372 | intergenic variant | T/C | snv | 0.54 | 3 | ||
rs1009080 | 1 | 29958713 | intergenic variant | G/A | snv | 0.54 | 2 | ||||
rs10949808 | 7 | 156255955 | intergenic variant | T/G | snv | 0.45 | 2 | ||||
rs1106076 | 1.000 | 0.080 | 7 | 5581212 | regulatory region variant | C/A;G | snv | 2 | |||
rs12527359 | 6 | 89018502 | intergenic variant | T/A | snv | 0.23 | 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 | ||||
rs2018368 | 11 | 10718819 | intergenic variant | C/G | snv | 0.59 | 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 | ||||
rs4680612 | 1.000 | 0.040 | 3 | 165891643 | intergenic variant | G/A | snv | 0.95 | 2 | ||
rs4996815 | 13 | 105999312 | intron variant | G/T | snv | 0.61 | 2 | ||||
rs6627057 | X | 145059799 | downstream gene variant | T/G | snv | 0.16 | 2 | ||||
rs7727102 | 5 | 4720472 | intron variant | G/C | snv | 0.32 | 2 |