Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10037512 | 5 | 89058858 | intron variant | T/A;C | snv | 2 | |||||
rs10901216 | 9 | 130596504 | intron variant | G/A | snv | 0.28 | 2 | ||||
rs118115924 | 12 | 48985754 | downstream gene variant | G/A;T | snv | 2 | |||||
rs1366594 | 5 | 89080244 | intron variant | A/C | snv | 0.57 | 2 | ||||
rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 2 | ||||
rs6894139 | 5 | 89031965 | non coding transcript exon variant | T/G | snv | 0.57 | 2 | ||||
rs6959212 | 7 | 38088724 | intergenic variant | T/C;G | snv | 2 | |||||
rs7466269 | 9 | 130588697 | intron variant | A/G | snv | 0.33 | 2 | ||||
rs9921222 | 0.925 | 0.120 | 16 | 325782 | intron variant | C/T | snv | 0.51 | 2 |