| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61736451 | 1.000 | 0.120 | 3 | 10359892 | missense variant | C/A;T | snv | 4.0E-06; 1.1E-02 | 1 | ||
| rs1250745641 | 1.000 | 0.120 | 10 | 71807866 | missense variant | G/A | snv | 1 | |||
| rs745434198 | 1.000 | 0.120 | 6 | 33165983 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs762356974 | 1.000 | 0.120 | 5 | 141573742 | missense variant | G/A;C;T | snv | 1.6E-05; 2.2E-05; 2.7E-05 | 1 | ||
| rs775146972 | 1.000 | 0.120 | 5 | 141573787 | missense variant | G/A;C | snv | 6.8E-06 | 1 | ||
| rs1348505504 | 1.000 | 0.120 | 19 | 3586669 | missense variant | G/A | snv | 7.4E-06 | 1 | ||
| rs11920109 | 1.000 | 0.120 | 3 | 7170999 | intron variant | T/C | snv | 0.35 | 1 | ||
| rs763320093 | 1.000 | 0.120 | 1 | 165203923 | missense variant | A/G | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs267606617 | 1.000 | 0.120 | MT | 1555 | non coding transcript exon variant | A/G | snv | 1 | |||
| rs4648011 | 1.000 | 0.120 | 4 | 102554287 | intron variant | G/T | snv | 0.61 | 1 | ||
| rs1131692056 | 1.000 | 0.120 | 16 | 23988577 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
| rs190166486 | 1.000 | 0.120 | 12 | 80539915 | missense variant | A/G | snv | 1.6E-04 | 6.3E-05 | 1 | |
| rs1322366495 | 1.000 | 0.120 | 12 | 80649626 | missense variant | A/G | snv | 1 | |||
| rs745927136 | 1.000 | 0.120 | 1 | 27102734 | missense variant | G/A | snv | 4.0E-05 | 1 | ||
| rs761976067 | 1.000 | 0.120 | 4 | 6301377 | missense variant | T/C;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs10258719 | 0.925 | 0.280 | 7 | 138771243 | missense variant | A/C;G;T | snv | 0.69 | 2 | ||
| rs549556142 | 0.925 | 0.120 | 1 | 100484347 | stop gained | C/A;T | snv | 1.6E-04; 4.1E-06 | 2 | ||
| rs876661408 | 0.925 | 0.120 | 1 | 100484440 | stop gained | C/T | snv | 4.3E-06 | 2 | ||
| rs876657776 | 0.925 | 0.160 | 5 | 141524167 | stop gained | G/A | snv | 2 | |||
| rs775097398 | 0.925 | 0.120 | 8 | 71216713 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs111033196 | 1.000 | 0.120 | 13 | 20189202 | missense variant | C/A;T | snv | 2.8E-04; 1.4E-02 | 2 | ||
| rs1291519904 | 0.925 | 0.120 | 13 | 20189325 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs397516875 | 0.925 | 0.120 | 13 | 20189197 | stop gained | C/A;T | snv | 6.4E-05 | 2 | ||
| rs11928865 | 1.000 | 0.120 | 3 | 7114015 | intron variant | T/A;G | snv | 2 | |||
| rs1391331735 | 0.925 | 0.120 | 17 | 18126795 | missense variant | C/T | snv | 7.0E-06 | 2 |