| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10046758 | 1.000 | 0.040 | 8 | 4326648 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
| rs10503256 | 1.000 | 0.040 | 8 | 4356657 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs11136775 | 0.925 | 0.040 | 8 | 4791194 | intron variant | G/C | snv | 0.12 | 2 | ||
| rs11779410 | 1.000 | 0.040 | 8 | 3015011 | intron variant | A/T | snv | 3.2E-02 | 1 | ||
| rs11787412 | 0.925 | 0.040 | 8 | 3276717 | intron variant | C/A;T | snv | 2 | |||
| rs11987640 | 1.000 | 8 | 4584258 | intron variant | G/C | snv | 0.12 | 2 | |||
| rs11998250 | 1.000 | 0.040 | 8 | 3162070 | intron variant | A/C | snv | 0.22 | 1 | ||
| rs12541020 | 1.000 | 0.040 | 8 | 4960070 | intron variant | T/A;C | snv | 1 | |||
| rs12550650 | 8 | 4693468 | intron variant | C/T | snv | 0.49 | 1 | ||||
| rs13250365 | 1.000 | 0.040 | 8 | 3155942 | intron variant | G/C;T | snv | 1 | |||
| rs13260434 | 0.925 | 0.040 | 8 | 3368702 | intron variant | T/A | snv | 0.24 | 2 | ||
| rs13261217 | 1.000 | 0.040 | 8 | 4325535 | non coding transcript exon variant | A/G | snv | 0.26 | 1 | ||
| rs13277378 | 1.000 | 0.040 | 8 | 3008416 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs1379326 | 8 | 4760288 | intron variant | T/C;G | snv | 1 | |||||
| rs139425113 | 1.000 | 0.040 | 8 | 4323090 | intron variant | A/-;AA;AAA | delins | 1 | |||
| rs142700918 | 0.925 | 0.080 | 8 | 3448320 | intron variant | G/A | snv | 5.8E-03 | 2 | ||
| rs145669495 | 8 | 4244902 | intron variant | A/G | snv | 1.6E-03 | 1 | ||||
| rs1460403 | 1.000 | 0.040 | 8 | 3162709 | intron variant | T/A | snv | 5.0E-02 | 1 | ||
| rs1658820 | 8 | 4431055 | intron variant | G/A;T | snv | 1 | |||||
| rs17079498 | 1.000 | 0.040 | 8 | 3160822 | intron variant | T/C | snv | 7.1E-02 | 1 | ||
| rs17079504 | 1.000 | 0.040 | 8 | 3161800 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs17079506 | 1.000 | 0.040 | 8 | 3162901 | intron variant | T/A | snv | 6.8E-02 | 1 | ||
| rs17079516 | 1.000 | 0.040 | 8 | 3166618 | intron variant | T/A;C | snv | 1 | |||
| rs17404163 | 8 | 4093523 | intron variant | A/G;T | snv | 1 |