| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3219493 | 0.882 | 0.120 | 1 | 45330597 | intron variant | G/C | snv | 0.92 | 0.93 | 3 | |
| rs1135612 | 0.882 | 0.120 | 7 | 75980359 | synonymous variant | A/G;T | snv | 0.28 | 3 | ||
| rs2228104 | 0.882 | 0.120 | 7 | 75985635 | synonymous variant | T/A;C | snv | 4.5E-06; 0.92 | 3 | ||
| rs7431 | 0.882 | 0.120 | 8 | 22540949 | 3 prime UTR variant | G/A | snv | 0.56 | 3 | ||
| rs1428779969 | 0.882 | 0.120 | 12 | 120223776 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs2074647 | 0.882 | 0.120 | 14 | 72562470 | missense variant | G/A | snv | 9.0E-02 | 0.10 | 3 | |
| rs17674580 | 0.882 | 0.120 | 18 | 45729946 | 5 prime UTR variant | C/A;T | snv | 3 | |||
| rs7832529 | 0.882 | 0.120 | 8 | 42449295 | intron variant | T/C | snv | 0.24 | 3 | ||
| rs11077654 | 0.882 | 0.120 | 17 | 73010373 | intron variant | A/C | snv | 0.69 | 3 | ||
| rs11871756 | 0.882 | 0.120 | 17 | 72730105 | intron variant | C/G | snv | 0.11 | 3 | ||
| rs4969054 | 0.882 | 0.120 | 17 | 73016334 | intron variant | G/C | snv | 0.73 | 3 | ||
| rs9913017 | 0.882 | 0.120 | 17 | 73014881 | intron variant | A/C;T | snv | 3 | |||
| rs1336331763 | 0.882 | 0.120 | 16 | 28606796 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs2664139 | 0.882 | 0.120 | 15 | 39580382 | upstream gene variant | T/C | snv | 0.41 | 3 | ||
| rs72552316 | 0.882 | 0.120 | X | 12889591 | 3 prime UTR variant | T/C | snv | 3 | |||
| rs377062126 | 0.882 | 0.120 | 12 | 104319543 | missense variant | G/A | snv | 2.1E-05 | 3.5E-05 | 3 | |
| rs3213255 | 0.882 | 0.120 | 19 | 43573355 | intron variant | G/A | snv | 0.60 | 3 | ||
| rs3213356 | 0.882 | 0.120 | 19 | 43554087 | intron variant | C/T | snv | 0.60 | 3 | ||
| rs861531 | 0.882 | 0.120 | 14 | 103706470 | 3 prime UTR variant | C/A | snv | 0.32 | 3 | ||
| rs1547651 | 0.851 | 0.200 | 6 | 43762907 | regulatory region variant | A/T | snv | 0.15 | 4 | ||
| rs2505568 | 0.851 | 0.160 | 10 | 36522408 | non coding transcript exon variant | T/A | snv | 0.56 | 4 | ||
| rs2764736 | 0.851 | 0.160 | 9 | 25067733 | intergenic variant | T/C | snv | 2.4E-02 | 4 | ||
| rs710521 | 0.851 | 0.200 | 3 | 189928144 | intergenic variant | T/C | snv | 0.24 | 4 | ||
| rs1046778 | 0.851 | 0.160 | 10 | 102901727 | 3 prime UTR variant | T/C | snv | 0.30 | 4 | ||
| rs353293 | 0.851 | 0.160 | 5 | 149427663 | non coding transcript exon variant | C/T | snv | 0.33 | 4 |