Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6696217 | 1 | 169491488 | non coding transcript exon variant | A/G | snv | 0.92 | 2 | ||||
rs7659024 | 4 | 154599778 | downstream gene variant | G/A | snv | 0.26 | 2 | ||||
rs970740 | 1 | 169510736 | downstream gene variant | C/T | snv | 0.95 | 2 | ||||
rs10476160 | 5 | 175547573 | regulatory region variant | A/G;T | snv | 1 | |||||
rs10746487 | 1 | 9278630 | intergenic variant | T/A;C | snv | 1 | |||||
rs10919507 | 1 | 170885468 | intron variant | C/T | snv | 3.0E-02 | 1 | ||||
rs113451833 | 8 | 64970119 | downstream gene variant | G/T | snv | 0.18 | 1 | ||||
rs115063924 | 1 | 168741790 | intron variant | C/A;T | snv | 6.7E-03 | 1 | ||||
rs12120558 | 1 | 170366687 | downstream gene variant | G/A | snv | 1.2E-02 | 1 | ||||
rs12136148 | 1 | 170123530 | intergenic variant | T/G | snv | 6.9E-02 | 1 | ||||
rs12450494 | 17 | 7304568 | upstream gene variant | T/A;C | snv | 1 | |||||
rs12981279 | 19 | 10528857 | intergenic variant | T/C | snv | 0.41 | 1 | ||||
rs142286129 | 11 | 54688761 | upstream gene variant | T/C | snv | 7.8E-03 | 1 | ||||
rs1423386 | 5 | 62689026 | intergenic variant | A/G | snv | 0.19 | 1 | ||||
rs143860577 | 11 | 50513762 | intergenic variant | A/T | snv | 7.3E-03 | 1 | ||||
rs144405847 | 1 | 82342193 | intron variant | C/T | snv | 4.9E-02 | 1 | ||||
rs147455989 | 11 | 50161397 | intergenic variant | T/C | snv | 7.8E-03 | 1 | ||||
rs148268781 | 11 | 50663948 | intergenic variant | T/A;C | snv | 1 | |||||
rs149903077 | 11 | 46328146 | upstream gene variant | G/T | snv | 9.5E-03 | 1 | ||||
rs181813804 | 11 | 48706704 | intergenic variant | A/G | snv | 8.1E-03 | 1 | ||||
rs182484222 | 11 | 48190205 | intergenic variant | G/A | snv | 7.7E-03 | 1 | ||||
rs182879407 | 11 | 47199227 | intergenic variant | C/G;T | snv | 1 | |||||
rs189484085 | 11 | 48511937 | upstream gene variant | C/T | snv | 8.1E-03 | 1 | ||||
rs190666382 | 11 | 54553509 | intergenic variant | C/A;T | snv | 1 | |||||
rs1910358 | 5 | 23907464 | intergenic variant | C/T | snv | 0.72 | 1 |