| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2596573 | 1.000 | 0.080 | 6 | 31380153 | upstream gene variant | C/T | snv | 0.75 | 1 | ||
| rs2747457 | 1.000 | 0.080 | 6 | 29688640 | intergenic variant | T/G | snv | 0.22 | 1 | ||
| rs3129073 | 1.000 | 0.080 | 6 | 29648045 | TF binding site variant | A/G | snv | 0.16 | 1 | ||
| rs7762933 | 1.000 | 0.080 | 6 | 31194743 | upstream gene variant | T/C | snv | 0.43 | 1 | ||
| rs974404 | 1.000 | 0.080 | 1 | 113839403 | intron variant | G/A;T | snv | 1 | |||
| rs2956467 | 1.000 | 0.080 | 12 | 48459456 | intergenic variant | G/A;C | snv | 1 | |||
| rs1655902 | 1.000 | 0.080 | 6 | 29949078 | downstream gene variant | G/A;C | snv | 1 | |||
| rs11090598 | 1.000 | 0.080 | 22 | 30125781 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs12167333 | 1.000 | 0.080 | 22 | 30179823 | downstream gene variant | C/T | snv | 0.21 | 1 | ||
| rs1978083 | 1.000 | 0.080 | 22 | 30174454 | intron variant | C/G | snv | 0.21 | 1 | ||
| rs4239933 | 1.000 | 0.080 | 22 | 30116425 | intron variant | C/G | snv | 0.21 | 1 | ||
| rs4337577 | 1.000 | 0.080 | 22 | 30116139 | intron variant | G/C | snv | 0.21 | 1 | ||
| rs7510705 | 1.000 | 0.080 | 22 | 30097929 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs8138286 | 1.000 | 0.080 | 22 | 30166998 | intron variant | A/C;G | snv | 0.20 | 1 | ||
| rs8141765 | 1.000 | 0.080 | 22 | 30166250 | intron variant | C/A;T | snv | 1 | |||
| rs9620953 | 1.000 | 0.080 | 22 | 30150256 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs9625919 | 1.000 | 0.080 | 22 | 30104969 | intron variant | G/T | snv | 0.21 | 1 | ||
| rs9625933 | 1.000 | 0.080 | 22 | 30159227 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs193473 | 1.000 | 0.080 | 22 | 30052410 | intron variant | A/G;T | snv | 1 | |||
| rs28257 | 1.000 | 0.080 | 22 | 30033126 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs41175 | 1.000 | 0.080 | 22 | 30036148 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs41178 | 1.000 | 0.080 | 22 | 30044544 | intron variant | G/A | snv | 0.28 | 1 | ||
| rs41179 | 1.000 | 0.080 | 22 | 30045688 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs8141404 | 1.000 | 0.080 | 22 | 30078227 | intron variant | C/T | snv | 0.21 | 1 | ||
| rs974494 | 1.000 | 0.080 | 22 | 26254399 | intron variant | C/G;T | snv | 1 |