| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10170218 | 1.000 | 0.040 | 2 | 187949717 | intron variant | A/C | snv | 0.25 | 1 | ||
| rs3100127 | 1.000 | 0.040 | 1 | 202191842 | upstream gene variant | C/A;T | snv | 1 | |||
| rs406001 | 1.000 | 0.040 | 7 | 51938719 | intergenic variant | T/A;C | snv | 1 | |||
| rs682457 | 1.000 | 0.040 | 11 | 88216364 | intergenic variant | T/C | snv | 0.14 | 1 | ||
| rs717947 | 1.000 | 0.040 | 4 | 33652135 | intron variant | C/A;T | snv | 1 | |||
| rs263232 | 1.000 | 0.040 | 8 | 130795923 | intron variant | C/A | snv | 6.7E-02 | 1 | ||
| rs10852889 | 1.000 | 0.040 | 17 | 6997526 | intron variant | C/A;G;T | snv | 1 | |||
| rs11599164 | 1.000 | 0.040 | 10 | 60072226 | missense variant | G/T | snv | 7.2E-02 | 7.3E-02 | 1 | |
| rs17208576 | 1.000 | 0.040 | 10 | 60074815 | synonymous variant | G/A | snv | 7.2E-02 | 7.3E-02 | 1 | |
| rs28932171 | 1.000 | 0.040 | 10 | 60071532 | missense variant | T/C | snv | 7.2E-02 | 7.3E-02 | 1 | |
| rs159572 | 1.000 | 0.040 | 5 | 56211219 | intron variant | A/C | snv | 0.37 | 1 | ||
| rs3852144 | 1.000 | 0.040 | 5 | 56566769 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs1990322 | 1.000 | 0.040 | 12 | 2651804 | intron variant | G/A | snv | 0.69 | 0.57 | 1 | |
| rs12898919 | 1.000 | 0.040 | 15 | 78588235 | intron variant | G/C | snv | 3.1E-02 | 1 | ||
| rs2267715 | 1.000 | 0.040 | 7 | 30676471 | intron variant | G/A;C | snv | 1 | |||
| rs16904179 | 1.000 | 0.040 | 8 | 129946705 | intron variant | G/A | snv | 6.2E-02 | 1 | ||
| rs10144436 | 1.000 | 0.040 | 14 | 95090065 | 3 prime UTR variant | C/A | snv | 2.9E-02 | 1 | ||
| rs2075652 | 1.000 | 0.040 | 11 | 113424176 | intron variant | G/A | snv | 4.2E-02 | 1 | ||
| rs2251177 | 1.000 | 0.040 | 3 | 114139503 | missense variant | C/A;T | snv | 8.0E-06; 0.99 | 1 | ||
| rs9868039 | 1.000 | 0.040 | 3 | 114127695 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs1374141592 | 1.000 | 0.040 | 5 | 180630561 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs58649573 | 1.000 | 0.040 | 9 | 124005148 | intron variant | T/C | snv | 1 | |||
| rs2400207 | 1.000 | 0.040 | 5 | 146000534 | intron variant | A/G | snv | 0.56 | 1 | ||
| rs12458282 | 1.000 | 0.040 | 18 | 77061897 | intron variant | T/C | snv | 0.24 | 1 | ||
| rs2074621 | 1.000 | 0.040 | 19 | 15179601 | non coding transcript exon variant | G/A | snv | 0.67 | 1 |