| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2430561 | 0.590 | 0.760 | 12 | 68158742 | intron variant | T/A | snv | 0.36 | 50 | ||
| rs2069705 | 0.695 | 0.440 | 12 | 68161231 | intron variant | G/A;C | snv | 19 | |||
| rs1861494 | 0.716 | 0.400 | 12 | 68157629 | intron variant | C/T | snv | 0.75 | 15 | ||
| rs2069718 | 0.742 | 0.320 | 12 | 68156382 | intron variant | A/G;T | snv | 0.50 | 14 | ||
| rs2069727 | 0.763 | 0.320 | 12 | 68154443 | intron variant | T/A;C | snv | 9 | |||
| rs1861493 | 0.851 | 0.280 | 12 | 68157416 | intron variant | G/A | snv | 0.76 | 4 | ||
| rs3138557 | 0.851 | 0.080 | 12 | 68158711 | intron variant | CGAG/- | delins | 4 | |||
| rs34079299 | 0.925 | 0.200 | 12 | 68158715 | intron variant | TGTGTGTGTGTG/-;TG;TGTG;TGTGTG;TGTGTGTG;TGTGTGTGTG;TGTGTGTGTGTGTG;TGTGTGTGTGTGTGTG;TGTGTGTGTGTGTGTGTG;TGTGTGTGTGTGTGTGTGTG;TGTGTGTGTGTGTGTGTGTGTG;TGTGTGTGTGTGTGTGTGTGTGTG;TGTGTGTGTGTGTGTGTGTGTGTGTG | delins | 2 | |||
| rs2069707 | 0.925 | 0.120 | 12 | 68160508 | intron variant | G/A;C | snv | 2 | |||
| rs2234688 | 1.000 | 0.040 | 12 | 68158742 | intron variant | -/G;TGAG;TGG;TGTGG;TGTGTGAG;TGTGTGG;TGTGTGTGG | delins | 1 | |||
| rs771694484 | 1.000 | 12 | 68157954 | missense variant | T/C | snv | 4.0E-05 | 7.0E-06 | 1 |