| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2072136 | 0.851 | 0.120 | 12 | 112961114 | synonymous variant | G/A;C | snv | 0.31; 4.0E-06 | 6 | ||
| rs2285932 | 0.851 | 0.120 | 12 | 112949145 | synonymous variant | T/C | snv | 0.76 | 0.78 | 5 | |
| rs2072134 | 12 | 112971371 | 3 prime UTR variant | G/A | snv | 3.7E-03 | 3 | ||||
| rs2072135 | 0.925 | 0.120 | 12 | 112961374 | intron variant | C/T | snv | 0.23 | 2 | ||
| rs6489882 | 0.925 | 0.120 | 12 | 112943571 | intron variant | G/A | snv | 0.75 | 2 | ||
| rs1859330 | 1.000 | 0.040 | 12 | 112938583 | missense variant | G/A;C;T | snv | 0.68 | 0.64 | 1 | |
| rs2010549 | 1.000 | 0.040 | 12 | 112971192 | 3 prime UTR variant | G/C;T | snv | 1 | |||
| rs2010604 | 1.000 | 0.040 | 12 | 112970403 | 3 prime UTR variant | G/C;T | snv | 1 | |||
| rs2240187 | 1.000 | 0.040 | 12 | 112966190 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs2240188 | 1.000 | 0.040 | 12 | 112965879 | missense variant | C/G;T | snv | 0.27 | 1 | ||
| rs2240189 | 1.000 | 0.040 | 12 | 112965692 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs4766678 | 1.000 | 0.040 | 12 | 112959886 | intron variant | G/A;C | snv | 1 | |||
| rs739903 | 1.000 | 0.040 | 12 | 112971069 | 3 prime UTR variant | A/G | snv | 0.25 | 1 | ||
| rs757404 | 1.000 | 0.040 | 12 | 112969387 | non coding transcript exon variant | G/A;C | snv | 1 | |||
| rs7961128 | 1.000 | 0.040 | 12 | 112947441 | intron variant | C/G;T | snv | 1 |