| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10498244 | 1.000 | 0.080 | 2 | 230173117 | non coding transcript exon variant | T/C | snv | 0.26 | 1 | ||
| rs1050504 | 1.000 | 0.080 | 8 | 58583857 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
| rs1057141 | 1.000 | 0.080 | 6 | 32850997 | missense variant | T/C | snv | 0.20 | 0.20 | 1 | |
| rs10841847 | 1.000 | 0.080 | 12 | 8535216 | intron variant | A/G | snv | 0.58 | 1 | ||
| rs11574079 | 1.000 | 0.080 | 12 | 47858947 | intron variant | C/T | snv | 1.7E-03 | 1 | ||
| rs11575886 | 1.000 | 0.080 | 20 | 56248494 | upstream gene variant | A/G | snv | 8.0E-02 | 1 | ||
| rs1371562 | 1.000 | 0.080 | 2 | 118975372 | intron variant | G/T | snv | 0.33 | 1 | ||
| rs141555015 | 1.000 | 0.080 | 6 | 32839023 | upstream gene variant | GCTTTGTAATTGGAGAAT/- | delins | 1.4E-05 | 1 | ||
| rs15493 | 1.000 | 0.080 | 14 | 67651415 | missense variant | C/G;T | snv | 9.2E-02 | 8.8E-02 | 1 | |
| rs1568952 | 1.000 | 0.080 | 8 | 58799804 | intergenic variant | T/C | snv | 0.75 | 1 | ||
| rs16826860 | 1.000 | 0.080 | 2 | 230182908 | intron variant | G/A | snv | 7.2E-02 | 1 | ||
| rs17009726 | 1.000 | 0.080 | 2 | 118967884 | intron variant | A/G | snv | 1.0E-02 | 1 | ||
| rs17795618 | 1.000 | 0.080 | 2 | 118973892 | intron variant | T/A | snv | 0.12 | 1 | ||
| rs1893352 | 1.000 | 0.080 | 11 | 126290792 | intron variant | A/C;G | snv | 1 | |||
| rs1927906 | 1.000 | 0.080 | 9 | 117717837 | 3 prime UTR variant | T/C | snv | 0.20 | 1 | ||
| rs2011839 | 1.000 | 0.080 | 2 | 118985008 | intron variant | C/A;T | snv | 1 | |||
| rs208290 | 1.000 | 0.080 | 12 | 121156253 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs2230424 | 1.000 | 0.080 | 16 | 31355997 | missense variant | T/C | snv | 8.6E-02 | 9.0E-02 | 1 | |
| rs2278589 | 1.000 | 0.080 | 2 | 118971300 | intron variant | G/A;C | snv | 1 | |||
| rs2660898 | 1.000 | 0.080 | 12 | 96032219 | intron variant | T/G | snv | 0.30 | 1 | ||
| rs2726600 | 1.000 | 0.080 | 8 | 58808045 | intron variant | G/A;C;T | snv | 1 | |||
| rs3092923 | 1.000 | 0.080 | X | 136659026 | intron variant | T/C | snv | 0.17 | 0.28 | 1 | |
| rs370738284 | 1.000 | 0.080 | 4 | 38797857 | synonymous variant | A/G | snv | 1.4E-05 | 1 | ||
| rs3774275 | 1.000 | 0.080 | 3 | 187247480 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs3819545 | 1.000 | 0.080 | 12 | 47871223 | intron variant | A/G | snv | 0.36 | 1 |