| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs537765533 | 0.882 | 0.080 | 2 | 113132839 | missense variant | G/C | snv | 2.0E-05 | 3 | ||
| rs6666258 | 0.882 | 0.080 | 1 | 154841792 | intron variant | G/C | snv | 0.30 | 3 | ||
| rs1490867890 | 0.882 | 0.080 | 1 | 150579475 | missense variant | G/A;C | snv | 3 | |||
| rs750805885 | 0.882 | 0.080 | 1 | 150579475 | frameshift variant | -/C | delins | 4.7E-06 | 3 | ||
| rs1056515 | 0.882 | 0.040 | 1 | 163143470 | 3 prime UTR variant | G/T | snv | 0.37 | 3 | ||
| rs539179964 | 0.882 | 0.080 | 8 | 104248720 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 3 | |
| rs79681911 | 0.882 | 0.040 | 11 | 18269755 | missense variant | G/A | snv | 2.1E-03 | 8.0E-04 | 3 | |
| rs7629265 | 0.882 | 0.080 | 3 | 38607330 | intron variant | C/T | snv | 2.3E-02 | 3 | ||
| rs1403934301 | 0.882 | 0.120 | 17 | 7631317 | missense variant | G/A | snv | 3 | |||
| rs1867624 | 0.851 | 0.080 | 17 | 64309731 | upstream gene variant | C/T | snv | 0.65 | 4 | ||
| rs4862423 | 0.882 | 0.080 | 4 | 184805394 | intron variant | C/T | snv | 0.37 | 4 | ||
| rs2518136 | 0.851 | 0.120 | 3 | 186620038 | intron variant | T/C | snv | 0.46 | 4 | ||
| rs12762303 | 0.851 | 0.080 | 10 | 45373723 | upstream gene variant | T/C | snv | 0.17 | 4 | ||
| rs200222843 | 0.851 | 0.120 | 2 | 21003286 | missense variant | G/A | snv | 4.0E-05 | 4.2E-05 | 4 | |
| rs1298417395 | 0.882 | 0.080 | 1 | 176206716 | missense variant | C/T | snv | 1.4E-05 | 4 | ||
| rs4845623 | 0.925 | 0.040 | 1 | 154443301 | intron variant | A/G | snv | 0.47 | 4 | ||
| rs4845617 | 0.882 | 0.080 | 1 | 154405422 | 5 prime UTR variant | G/A;C | snv | 4 | |||
| rs755460305 | 0.882 | 0.080 | 3 | 186732650 | missense variant | C/A | snv | 4 | |||
| rs879254582 | 0.851 | 0.160 | 19 | 11105488 | frameshift variant | AGCCCCT/- | delins | 4 | |||
| rs797044485 | 0.851 | 0.160 | 1 | 156134832 | missense variant | G/A | snv | 4 | |||
| rs33932899 | 0.851 | 0.240 | 16 | 11254354 | intron variant | C/G;T | snv | 4 | |||
| rs121918313 | 0.851 | 0.080 | 12 | 12164494 | missense variant | G/A | snv | 1.6E-05 | 4 | ||
| rs3736234 | 0.851 | 0.040 | 12 | 10160535 | non coding transcript exon variant | G/A | snv | 0.40 | 4 | ||
| rs773297988 | 0.882 | 0.080 | 3 | 138698965 | missense variant | T/C | snv | 4.0E-06 | 3.5E-05 | 4 | |
| rs755725121 | 0.882 | 0.080 | 1 | 9716029 | missense variant | G/A | snv | 2.1E-05 | 7.0E-06 | 4 |