| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11742570 | 0.925 | 0.040 | 5 | 40410482 | upstream gene variant | T/C;G | snv | 3 | |||
| rs12103 | 0.925 | 0.040 | 1 | 1312114 | synonymous variant | T/A;C;G | snv | 0.56 | 3 | ||
| rs1250569 | 0.925 | 0.040 | 10 | 79285450 | intron variant | T/C | snv | 0.44 | 0.51 | 3 | |
| rs1292975971 | 0.925 | 0.040 | 16 | 50711664 | synonymous variant | C/T | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs13300218 | 0.925 | 0.040 | 9 | 136505189 | intron variant | G/A | snv | 7.5E-02 | 3 | ||
| rs1333407770 | 0.925 | 0.040 | 10 | 77811115 | frameshift variant | G/-;GG | delins | 3 | |||
| rs142430606 | 0.925 | 0.040 | 22 | 49998059 | missense variant | G/A;T | snv | 1.1E-02; 4.4E-06 | 3 | ||
| rs1474156473 | 0.925 | 0.040 | 2 | 233293259 | synonymous variant | T/C | snv | 7.0E-06 | 3 | ||
| rs1523127 | 0.925 | 0.040 | 3 | 119782192 | 5 prime UTR variant | C/A | snv | 0.48 | 3 | ||
| rs17694108 | 0.925 | 0.040 | 19 | 33240645 | regulatory region variant | G/A | snv | 0.22 | 3 | ||
| rs200550971 | 0.925 | 0.040 | 6 | 88144985 | missense variant | T/C | snv | 3.6E-05 | 1.4E-05 | 3 | |
| rs200711300 | 0.925 | 0.040 | 18 | 12802118 | missense variant | A/C;G | snv | 1.6E-04; 4.0E-06 | 3 | ||
| rs2189234 | 1.000 | 0.040 | 4 | 105154341 | intron variant | T/G | snv | 0.62 | 3 | ||
| rs2276707 | 0.925 | 0.040 | 3 | 119815306 | intron variant | C/G;T | snv | 4.1E-04; 0.24 | 3 | ||
| rs2289310 | 0.925 | 0.040 | 10 | 77811115 | missense variant | G/A;C;T | snv | 4.0E-06; 8.0E-06; 5.7E-02 | 3 | ||
| rs2294881 | 1.000 | 0.040 | 6 | 32399827 | intron variant | T/C | snv | 0.19 | 3 | ||
| rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 3 | ||
| rs2413583 | 0.925 | 0.040 | 22 | 39263768 | intron variant | C/T | snv | 0.19 | 3 | ||
| rs2488389 | 0.925 | 0.040 | 1 | 197662011 | intron variant | G/A | snv | 0.22 | 3 | ||
| rs2823286 | 0.925 | 0.040 | 21 | 15445619 | intron variant | G/A | snv | 0.28 | 3 | ||
| rs2930047 | 0.925 | 0.040 | 5 | 10695414 | intron variant | T/C | snv | 0.49 | 3 | ||
| rs3212217 | 0.925 | 0.040 | 5 | 159328122 | intron variant | C/G | snv | 0.26 | 3 | ||
| rs35873774 | 0.925 | 0.040 | 22 | 28795944 | intron variant | A/G | snv | 4.6E-02 | 3 | ||
| rs3742130 | 0.925 | 0.040 | 13 | 99255087 | synonymous variant | G/A | snv | 0.16 | 0.16 | 3 | |
| rs3745635 | 0.882 | 0.040 | 19 | 5844332 | missense variant | C/T | snv | 8.5E-02 | 0.11 | 3 |