| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs730881687 | 1.000 | 0.080 | 22 | 28710060 | splice acceptor variant | C/A;T | snv | 1.2E-05; 1.6E-05 | 2 | ||
| rs1262069856 | 1.000 | 0.080 | 2 | 214728724 | stop gained | C/T | snv | 1 | |||
| rs1296005499 | 1.000 | 0.080 | 17 | 43045746 | missense variant | C/T | snv | 1 | |||
| rs139399785 | 1.000 | 0.080 | 1 | 226380111 | stop gained | G/A;T | snv | 4.0E-06; 2.6E-04 | 1 | ||
| rs2227945 | 1.000 | 0.080 | 17 | 43092113 | missense variant | T/C;G | snv | 2.5E-03 | 1.0E-02 | 1 | |
| rs35628 | 1.000 | 0.080 | 16 | 16077249 | intron variant | A/G | snv | 0.13 | 1 | ||
| rs377294979 | 1.000 | 0.080 | 19 | 48961574 | missense variant | G/A;C | snv | 3.7E-05; 4.1E-06 | 1 | ||
| rs587782462 | 1.000 | 0.080 | 16 | 23641140 | synonymous variant | C/A;T | snv | 1 | |||
| rs61754118 | 1.000 | 0.080 | 2 | 214728798 | missense variant | T/C | snv | 7.7E-03 | 7.4E-03 | 1 | |
| rs758814202 | 1.000 | 0.080 | 10 | 126066725 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
| rs876660825 | 1.000 | 0.080 | 17 | 7674962 | missense variant | G/A;C | snv | 1 | |||
| rs762292600 | 0.925 | 0.080 | 6 | 151944316 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 7 | |
| rs200863613 | 0.925 | 0.080 | 9 | 21971061 | missense variant | C/A;T | snv | 8.5E-05 | 3.7E-04 | 6 | |
| rs752295912 | 0.925 | 0.080 | 17 | 39710398 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
| rs11544331 | 0.925 | 0.080 | 7 | 1091775 | missense variant | C/T | snv | 0.21 | 0.19 | 5 | |
| rs180177111 | 0.925 | 0.080 | 16 | 23629831 | stop gained | G/A | snv | 4.0E-06 | 5 | ||
| rs368094521 | 0.925 | 0.120 | 17 | 39724861 | missense variant | G/A | snv | 1.2E-03 | 2.6E-04 | 5 | |
| rs570613 | 0.925 | 0.080 | 10 | 8064539 | intron variant | C/T | snv | 0.60 | 5 | ||
| rs10109984 | 0.925 | 0.080 | 8 | 47891114 | intron variant | T/C | snv | 0.54 | 4 | ||
| rs1056123575 | 0.925 | 0.080 | 21 | 26844557 | missense variant | G/A | snv | 4.2E-06 | 7.0E-06 | 4 | |
| rs1114167628 | 0.925 | 0.080 | 10 | 87961033 | stop gained | -/ATATCTAG | delins | 4 | |||
| rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 4 | |
| rs1172398253 | 0.925 | 0.080 | 1 | 85582045 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
| rs11780156 | 0.925 | 0.080 | 8 | 128182395 | intron variant | C/T | snv | 0.13 | 4 | ||
| rs11895168 | 0.925 | 0.080 | 2 | 211377467 | 3 prime UTR variant | A/C | snv | 0.68 | 4 |