Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2999393 | 14 | 51188449 | intergenic variant | G/T | snv | 0.71 | 1 | ||||
rs3007168 | 14 | 51141575 | intergenic variant | G/A | snv | 0.15 | 1 | ||||
rs3093077 | 0.827 | 0.200 | 1 | 159709846 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs3134906 | 7 | 142807470 | downstream gene variant | G/A | snv | 0.56 | 1 | ||||
rs3763608 | 9 | 69032459 | upstream gene variant | T/C | snv | 0.37 | 1 | ||||
rs4121859 | 11 | 95444976 | regulatory region variant | C/T | snv | 0.20 | 1 | ||||
rs4281045 | 7 | 142810692 | downstream gene variant | C/A | snv | 0.20 | 1 | ||||
rs450533 | 4 | 106909104 | intron variant | T/C | snv | 0.36 | 1 | ||||
rs4553443 | 12 | 54929761 | intergenic variant | T/A;G | snv | 1 | |||||
rs4594175 | 14 | 51139823 | regulatory region variant | C/A | snv | 0.33 | 1 | ||||
rs4794031 | 17 | 49264791 | intron variant | C/A;T | snv | 1 | |||||
rs4817642 | 21 | 34312702 | intron variant | G/A | snv | 0.48 | 1 | ||||
rs5029614 | 6 | 18100143 | intergenic variant | A/G | snv | 0.32 | 1 | ||||
rs534126 | 7 | 143224141 | non coding transcript exon variant | C/G;T | snv | 1 | |||||
rs538592 | 11 | 95367983 | regulatory region variant | C/T | snv | 0.75 | 1 | ||||
rs62355900 | 1.000 | 0.040 | 5 | 56756868 | regulatory region variant | T/C | snv | 0.15 | 1 | ||
rs659119 | 6 | 149212011 | intergenic variant | C/T | snv | 0.17 | 1 | ||||
rs6946770 | 7 | 142693973 | upstream gene variant | A/G;T | snv | 1 | |||||
rs6975391 | 7 | 142662001 | upstream gene variant | T/A;C;G | snv | 1 | |||||
rs7148539 | 14 | 51168554 | regulatory region variant | C/A;T | snv | 1 | |||||
rs8129326 | 21 | 34440329 | intergenic variant | A/G | snv | 1 | |||||
rs9323205 | 14 | 51119749 | regulatory region variant | A/G | snv | 0.21 | 1 | ||||
rs9376307 | 6 | 137962128 | intron variant | C/T | snv | 0.28 | 1 | ||||
rs9599474 | 13 | 34721318 | intergenic variant | A/G | snv | 0.14 | 1 | ||||
rs971535 | 11 | 23123974 | regulatory region variant | C/T | snv | 0.46 | 1 |