| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 3 | |
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 3 | ||
| rs505151 | 0.732 | 0.360 | 1 | 55063514 | missense variant | G/A | snv | 0.95 | 0.90 | 3 | |
| rs4951074 | 1.000 | 0.040 | 1 | 203691653 | intron variant | A/G;T | snv | 2 | |||
| rs10900585 | 1.000 | 0.040 | 1 | 203684896 | intron variant | G/T | snv | 0.81 | 1 | ||
| rs12405994 | 1.000 | 0.040 | 1 | 75969735 | intron variant | A/C;T | snv | 1 | |||
| rs1417402 | 1.000 | 0.040 | 1 | 75971511 | intron variant | G/A | snv | 7.1E-02 | 1 | ||
| rs2274567 | 0.776 | 0.400 | 1 | 207580276 | missense variant | A/G | snv | 0.25 | 0.21 | 1 | |
| rs2296160 | 0.925 | 0.120 | 1 | 207621975 | missense variant | A/G | snv | 0.82 | 0.81 | 1 | |
| rs10192428 | 1.000 | 0.040 | 2 | 231014025 | 3 prime UTR variant | G/A | snv | 0.44 | 1 | ||
| rs1543061 | 1.000 | 0.040 | 2 | 231013781 | intron variant | C/T | snv | 0.44 | 1 | ||
| rs6755404 | 1.000 | 0.040 | 2 | 184932501 | intron variant | A/C | snv | 0.82 | 1 | ||
| rs488069 | 0.925 | 0.080 | 3 | 43090952 | intron variant | C/T | snv | 0.79 | 1 | ||
| rs5743810 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 1 | |
| rs316414 | 1.000 | 0.040 | 5 | 43004178 | downstream gene variant | A/G | snv | 0.67 | 1 | ||
| rs3211938 | 0.882 | 0.200 | 7 | 80671133 | stop gained | T/G | snv | 6.2E-03 | 2.6E-02 | 2 | |
| rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 12 | |||
| rs8176693 | 0.851 | 0.160 | 9 | 133262254 | intron variant | C/T | snv | 9.9E-02 | 5 | ||
| rs8176749 | 1.000 | 0.040 | 9 | 133255801 | synonymous variant | C/T | snv | 0.12 | 0.11 | 4 | |
| rs77641731 | 1.000 | 0.040 | 9 | 133257521 | missense variant | T/C | snv | 3 | |||
| rs7855466 | 0.925 | 0.080 | 9 | 133245916 | downstream gene variant | C/T | snv | 0.23 | 3 | ||
| rs8176719 | 0.925 | 0.120 | 9 | 133257521 | frameshift variant | -/C | ins | 0.37 | 0.35 | 3 | |
| rs8176722 | 1.000 | 0.040 | 9 | 133257367 | intron variant | C/A | snv | 0.13 | 0.12 | 3 |