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 | 62 | ||
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
rs17251221 | 0.724 | 0.360 | 3 | 122274400 | intron variant | A/G | snv | 0.11 | 18 | ||
rs9895661 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 10 | ||
rs13083990 | 0.925 | 0.080 | 3 | 122295719 | downstream gene variant | T/C | snv | 0.30 | 4 | ||
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 4 | ||
rs10934578 | 0.925 | 0.080 | 3 | 122258435 | intron variant | G/T | snv | 0.30 | 4 | ||
rs17265703 | 3 | 122329797 | intron variant | A/G | snv | 0.12 | 4 | ||||
rs1570669 | 0.925 | 0.080 | 20 | 54157888 | intron variant | A/G | snv | 0.42 | 4 | ||
rs1550532 | 2 | 233356202 | intron variant | C/G | snv | 0.75 | 4 | ||||
rs10934582 | 3 | 122294507 | downstream gene variant | G/A | snv | 0.28 | 3 | ||||
rs2270859 | 1.000 | 0.040 | 3 | 122536861 | non coding transcript exon variant | G/A | snv | 0.14 | 3 | ||
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 | ||||
rs6123359 | 1.000 | 0.080 | 20 | 54098167 | regulatory region variant | A/G | 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 |