Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13394720 | 1.000 | 2 | 233593475 | intergenic variant | T/C | snv | 7.0E-02 | 6 | |||
rs2741027 | 1.000 | 0.040 | 2 | 233609365 | downstream gene variant | G/A | snv | 0.22 | 4 | ||
rs17864661 | 2 | 233587096 | downstream gene variant | C/T | snv | 0.14 | 3 | ||||
rs2602362 | 2 | 233607902 | downstream gene variant | A/C | snv | 0.22 | 3 | ||||
rs2602363 | 2 | 233611879 | intergenic variant | T/C | snv | 0.22 | 3 | ||||
rs2602364 | 2 | 233615583 | upstream gene variant | G/A | snv | 0.22 | 3 | ||||
rs2741019 | 2 | 233602042 | upstream gene variant | C/A;G | snv | 3 | |||||
rs2741021 | 2 | 233603237 | upstream gene variant | C/T | snv | 0.22 | 3 | ||||
rs2741028 | 2 | 233610268 | intergenic variant | G/A;T | snv | 3 | |||||
rs10164928 | 2 | 233893139 | regulatory region variant | C/T | snv | 5.8E-02 | 2 | ||||
rs10175828 | 2 | 233473171 | downstream gene variant | G/C;T | snv | 2 | |||||
rs10841642 | 12 | 20791740 | intergenic variant | C/A;T | snv | 2 | |||||
rs10841645 | 12 | 20795800 | intergenic variant | A/C | snv | 0.59 | 2 | ||||
rs10841648 | 12 | 20801623 | intergenic variant | C/A;T | snv | 2 | |||||
rs11045505 | 12 | 20796512 | intergenic variant | C/T | snv | 0.59 | 2 | ||||
rs1115381 | 2 | 233596639 | intergenic variant | T/C | snv | 0.71 | 2 | ||||
rs11890203 | 2 | 233871485 | upstream gene variant | A/G | snv | 0.14 | 2 | ||||
rs12313384 | 12 | 20790827 | intergenic variant | G/T | snv | 0.58 | 2 | ||||
rs12549576 | 8 | 111963912 | intergenic variant | A/G | snv | 4.0E-02 | 2 | ||||
rs12618259 | 2 | 233598275 | intergenic variant | A/T | snv | 0.22 | 2 | ||||
rs12823467 | 12 | 20790642 | intergenic variant | T/C | snv | 0.59 | 2 | ||||
rs13383300 | 2 | 233586823 | downstream gene variant | C/A;G | snv | 2 | |||||
rs13387539 | 2 | 233573964 | intergenic variant | C/T | snv | 5.1E-02 | 2 | ||||
rs13394291 | 2 | 233593094 | intergenic variant | T/C | snv | 8.8E-02 | 2 | ||||
rs1551286 | 2 | 233606509 | downstream gene variant | C/G;T | snv | 2 |