Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs17265703 | 3 | 122329797 | intron variant | A/G | snv | 0.12 | 4 | ||||
rs1550532 | 2 | 233356202 | intron variant | C/G | snv | 0.75 | 4 | ||||
rs9895661 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 3 | ||
rs10934582 | 3 | 122294507 | downstream gene variant | G/A | snv | 0.28 | 2 | ||||
rs13083990 | 0.925 | 0.080 | 3 | 122295719 | downstream gene variant | T/C | snv | 0.30 | 2 | ||
rs13085498 | 3 | 122292516 | downstream gene variant | C/A;T | snv | 0.28 | 2 | ||||
rs13085674 | 3 | 122292504 | downstream gene variant | G/A | snv | 0.28 | 2 | ||||
rs1402200 | 3 | 122303570 | intergenic variant | G/A;C | snv | 2 | |||||
rs1472621 | 3 | 122293879 | downstream gene variant | A/G | snv | 0.28 | 2 | ||||
rs16832956 | 3 | 122298661 | regulatory region variant | C/G;T | snv | 0.19 | 2 | ||||
rs17711722 | 7 | 65806210 | downstream gene variant | C/T | snv | 2 | |||||
rs2001548 | 3 | 122313942 | upstream gene variant | G/A | snv | 0.12 | 2 | ||||
rs4678180 | 3 | 122318950 | downstream gene variant | T/C | snv | 0.62 | 2 | ||||
rs5008830 | 3 | 122311615 | intergenic variant | G/A | snv | 0.12 | 2 | ||||
rs6438720 | 3 | 122298385 | TF binding site variant | A/C | snv | 0.60 | 2 | ||||
rs6803098 | 3 | 122321763 | upstream gene variant | C/T | snv | 0.62 | 2 | ||||
rs9851884 | 3 | 122301347 | regulatory region variant | A/G | snv | 0.66 | 2 | ||||
rs9864290 | 3 | 122321215 | upstream gene variant | C/T | snv | 0.62 | 2 | ||||
rs11967485 | 6 | 156807123 | intron variant | G/A | snv | 0.15 | 2 | ||||
rs7481584 | 11 | 3007859 | non coding transcript exon variant | G/A | snv | 0.27 | 2 | ||||
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 2 | ||
rs10934578 | 0.925 | 0.080 | 3 | 122258435 | intron variant | G/T | snv | 0.30 | 2 | ||
rs12635478 | 3 | 122289706 | 3 prime UTR variant | C/A | snv | 0.28 | 2 | ||||
rs13095172 | 3 | 122271410 | intron variant | C/T | snv | 0.28 | 2 |