| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17684886 | 0.925 | 0.160 | 16 | 75052977 | intron variant | A/T | snv | 0.12 | 2 | ||
| rs2115386 | 0.925 | 0.160 | 19 | 7196554 | intron variant | C/T | snv | 0.48 | 2 | ||
| rs3751624 | 1.000 | 0.120 | 15 | 52282973 | intron variant | C/T | snv | 0.20 | 2 | ||
| rs3913535 | 0.925 | 0.160 | 11 | 89363589 | intron variant | T/C | snv | 0.30 | 2 | ||
| rs507392 | 0.925 | 0.160 | 7 | 100722313 | intron variant | G/A;C | snv | 2 | |||
| rs6060566 | 0.925 | 0.160 | 20 | 35700304 | intron variant | T/C | snv | 0.19 | 2 | ||
| rs899036 | 0.925 | 0.160 | 11 | 41661360 | intron variant | G/T | snv | 0.77 | 2 | ||
| rs10491034 | 1.000 | 0.120 | 10 | 48602322 | intron variant | G/A;T | snv | 1 | |||
| rs11567245 | 1.000 | 0.120 | 7 | 82151406 | intron variant | T/A | snv | 1 | |||
| rs12656571 | 1.000 | 0.120 | 5 | 109742339 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs13163610 | 1.000 | 0.120 | 5 | 94213172 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs139876191 | 1.000 | 0.120 | 6 | 34242693 | intron variant | -/C | delins | 7.7E-02; 5.8E-06 | 5.2E-02 | 1 | |
| rs142293996 | 1.000 | 0.120 | 1 | 224260357 | intron variant | C/A | snv | 1.1E-02 | 1 | ||
| rs148995025 | 1.000 | 0.120 | 5 | 7085094 | intron variant | A/G | snv | 8.9E-03 | 1 | ||
| rs1535724 | 1.000 | 0.120 | 13 | 75609137 | intron variant | G/C;T | snv | 1 | |||
| rs1711347 | 1.000 | 0.120 | 1 | 243998680 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs17376456 | 1.000 | 0.120 | 5 | 94221997 | intron variant | A/G | snv | 8.7E-02 | 1 | ||
| rs2031236 | 1.000 | 0.120 | 13 | 75595641 | intron variant | G/A;T | snv | 1 | |||
| rs2038823 | 1.000 | 0.120 | 13 | 96299179 | intron variant | G/A;T | snv | 1 | |||
| rs2070682 | 1.000 | 0.120 | 7 | 101133986 | intron variant | T/C | snv | 0.44 | 1 | ||
| rs227453 | 1.000 | 0.120 | 6 | 165065309 | intron variant | A/T | snv | 0.18 | 1 | ||
| rs227455 | 1.000 | 0.120 | 6 | 165064562 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs2300993 | 1.000 | 0.120 | 5 | 109702928 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs2328963 | 1.000 | 0.120 | 13 | 75601390 | intron variant | C/A;T | snv | 1 | |||
| rs2328964 | 1.000 | 0.120 | 13 | 75564694 | intron variant | G/T | snv | 0.79 | 1 |