| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 11 | ||
| rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 10 | |||
| rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 10 | |||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
| rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 5 | ||
| rs12123821 | 0.925 | 0.080 | 1 | 152206676 | intron variant | C/T | snv | 2.9E-02 | 4 | ||
| rs2070901 | 0.882 | 0.120 | 1 | 161215268 | non coding transcript exon variant | G/T | snv | 0.32 | 4 | ||
| rs1102705 | 0.925 | 0.080 | 1 | 172731728 | intergenic variant | G/A | snv | 0.93 | 3 | ||
| rs115288876 | 0.925 | 0.120 | 1 | 152027641 | intron variant | G/A | snv | 2.5E-02 | 3 | ||
| rs1214598 | 0.925 | 0.120 | 1 | 167457187 | non coding transcript exon variant | G/A;C;T | snv | 3 | |||
| rs301805 | 1.000 | 0.080 | 1 | 8420956 | intron variant | T/G | snv | 0.65 | 3 | ||
| rs301819 | 0.882 | 0.120 | 1 | 8441726 | intron variant | A/G;T | snv | 3 | |||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 3 | |
| rs7518129 | 0.882 | 0.120 | 1 | 173194429 | intron variant | A/G | snv | 0.47 | 3 | ||
| rs7528684 | 0.752 | 0.560 | 1 | 157701026 | upstream gene variant | A/G | snv | 0.57 | 3 | ||
| rs10158467 | 0.925 | 0.080 | 1 | 173162354 | regulatory region variant | A/G;T | snv | 2 | |||
| rs10789340 | 0.925 | 0.120 | 1 | 72474590 | intron variant | A/G;T | snv | 2 | |||
| rs11584383 | 0.827 | 0.200 | 1 | 200966738 | downstream gene variant | T/C | snv | 0.24 | 2 | ||
| rs12023876 | 0.925 | 0.080 | 1 | 203124073 | intron variant | G/A;T | snv | 2 | |||
| rs12743520 | 1.000 | 0.080 | 1 | 92571555 | intron variant | C/A | snv | 0.20 | 2 | ||
| rs1617333 | 0.925 | 0.080 | 1 | 167467033 | intron variant | A/G | snv | 0.27 | 2 | ||
| rs17668708 | 0.925 | 0.080 | 1 | 198671359 | intron variant | C/T | snv | 8.0E-02 | 2 |