| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
| rs7005606 | 0.925 | 0.080 | 8 | 32543983 | intron variant | T/G | snv | 0.39 | 3 | ||
| rs7826312 | 8 | 32542597 | intron variant | T/C | snv | 0.57 | 2 | ||||
| rs4236709 | 0.925 | 0.080 | 8 | 32552592 | intron variant | G/A;T | snv | 2 | |||
| rs1878918 | 0.925 | 0.120 | 8 | 32476054 | intron variant | G/A;C | snv | 2 | |||
| rs16879552 | 0.882 | 0.080 | 8 | 32553698 | intron variant | C/T | snv | 0.10 | 2 | ||
| rs7820838 | 1.000 | 0.040 | 8 | 32548461 | 5 prime UTR variant | T/A;C | snv | 2 | |||
| rs7825175 | 8 | 32558756 | intron variant | G/A | snv | 0.18 | 2 | ||||
| rs6996585 | 0.925 | 0.080 | 8 | 32543285 | intron variant | A/G | snv | 0.37 | 2 | ||
| rs77752517 | 8 | 32523661 | intron variant | C/G;T | snv | 1 | |||||
| rs4489283 | 8 | 32542144 | intron variant | T/C | snv | 0.59 | 1 | ||||
| rs10102889 | 8 | 32578102 | intron variant | C/G | snv | 9.0E-02 | 1 | ||||
| rs2466075 | 1.000 | 0.040 | 8 | 32575431 | intron variant | A/G | snv | 0.51 | 1 | ||
| rs35033136 | 8 | 32744536 | intron variant | C/A;T | snv | 1 | |||||
| rs7000590 | 8 | 32543110 | intron variant | T/C | snv | 0.73 | 1 | ||||
| rs2466077 | 8 | 32575235 | intron variant | G/T | snv | 0.53 | 1 | ||||
| rs2439302 | 0.776 | 0.200 | 8 | 32574851 | intron variant | G/C | snv | 0.54 | 1 | ||
| rs2466076 | 1.000 | 0.080 | 8 | 32575278 | intron variant | G/T | snv | 0.53 | 1 | ||
| rs527953512 | 8 | 32533038 | intron variant | A/-;AA;AAA;AAAA;AAAAAA | delins | 1 | |||||
| rs2466103 | 8 | 32554786 | intron variant | T/A;G | snv | 1 | |||||
| rs200393053 | 8 | 32736709 | intron variant | T/-;TT | delins | 1 | |||||
| rs10088648 | 1.000 | 8 | 32523319 | intron variant | A/T | snv | 0.56 | 1 | |||
| rs1481757 | 8 | 32110442 | intron variant | T/C | snv | 0.72 | 1 |