Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs9829896 | 3 | 20135980 | intron variant | C/A;T | snv | 2 | |||||
rs2377339 | 2 | 105840835 | intron variant | A/G | snv | 4.8E-02 | 2 | ||||
rs12043259 | 1 | 204858913 | intron variant | C/G | snv | 0.11 | 2 | ||||
rs12284594 | 1.000 | 0.080 | 11 | 125309957 | intron variant | A/G;T | snv | 2 | |||
rs118129027 | 7 | 39545812 | non coding transcript exon variant | T/C | snv | 3.5E-02 | 1 | ||||
rs1417205 | 13 | 47324744 | intergenic variant | A/G | snv | 0.13 | 1 | ||||
rs12995333 | 2 | 105819909 | intron variant | G/T | snv | 0.30 | 1 | ||||
rs12995849 | 2 | 105826655 | intron variant | C/T | snv | 0.63 | 1 | ||||
rs1465639 | 2 | 105822725 | intron variant | T/C | snv | 0.32 | 1 | ||||
rs1465641 | 2 | 105822480 | intron variant | C/G;T | snv | 1 | |||||
rs2163349 | 2 | 105841192 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs2163350 | 2 | 105828825 | intron variant | A/C;G | snv | 1 | |||||
rs4851095 | 2 | 105839093 | intron variant | T/C | snv | 0.94 | 1 | ||||
rs4851870 | 2 | 105820800 | intron variant | C/T | snv | 0.20 | 1 | ||||
rs6741172 | 2 | 105823603 | intron variant | A/G | snv | 0.32 | 1 | ||||
rs6747023 | 2 | 105815399 | intron variant | A/G;T | snv | 1 | |||||
rs7589342 | 2 | 105817021 | intron variant | C/T | snv | 0.28 | 1 | ||||
rs7589561 | 2 | 105837629 | intron variant | C/G;T | snv | 1 |