| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10480300 | 0.925 | 0.120 | 7 | 151708919 | intron variant | C/T | snv | 0.24 | 4 | ||
| rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 4 | ||
| rs12113155 | 7 | 151607887 | intron variant | A/C;G | snv | 3 | |||||
| rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 2 | ||
| rs1881626 | 7 | 151825722 | intron variant | T/C | snv | 0.96 | 2 | ||||
| rs7805747 | 1.000 | 0.080 | 7 | 151710715 | intron variant | G/A | snv | 0.26 | 2 | ||
| rs17173197 | 1.000 | 0.120 | 7 | 151571834 | non coding transcript exon variant | C/T | snv | 0.34 | 1 | ||
| rs10480299 | 7 | 151708732 | intron variant | T/C | snv | 0.26 | 1 | ||||
| rs11983465 | 7 | 151699885 | intron variant | C/G;T | snv | 1 | |||||
| rs6967838 | 7 | 151700602 | intron variant | T/C | snv | 0.30 | 1 | ||||
| rs6967507 | 7 | 151700401 | intron variant | T/C | snv | 0.22 | 1 | ||||
| rs6948449 | 7 | 151701047 | intron variant | C/T | snv | 0.20 | 1 | ||||
| rs6947707 | 7 | 151700687 | intron variant | A/T | snv | 0.29 | 1 | ||||
| rs6947064 | 7 | 151700257 | intron variant | A/G;T | snv | 1 | |||||
| rs6947912 | 7 | 151700559 | intron variant | G/C | snv | 0.22 | 1 | ||||
| rs2374270 | 7 | 151705704 | intron variant | C/A | snv | 0.36 | 1 |