| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs139660738 | 1.000 | 0.040 | 12 | 94791412 | intergenic variant | T/C | snv | 6.3E-03 | 1 | ||
| rs141480664 | 1.000 | 0.040 | 7 | 4469958 | regulatory region variant | G/A | snv | 1.0E-02 | 1 | ||
| rs142609537 | 1.000 | 0.040 | 15 | 95675665 | intron variant | A/G | snv | 1.8E-02 | 1 | ||
| rs146594485 | 1.000 | 0.040 | 20 | 3776090 | downstream gene variant | G/A | snv | 6.1E-03 | 1 | ||
| rs149969998 | 1.000 | 0.040 | 17 | 13692262 | intergenic variant | G/C;T | snv | 1 | |||
| rs150418526 | 1.000 | 0.040 | 17 | 38697587 | upstream gene variant | C/G;T | snv | 1 | |||
| rs150616616 | 1.000 | 0.040 | 5 | 121366663 | downstream gene variant | C/G;T | snv | 1 | |||
| rs150759334 | 1.000 | 0.040 | 4 | 60800528 | downstream gene variant | T/C | snv | 9.4E-03 | 1 | ||
| rs150828104 | 1.000 | 0.040 | 12 | 116337891 | regulatory region variant | TTTTGTTTTG/-;TTTTG;TTTTGTTTTGTTTTG;TTTTGTTTTGTTTTGTTTTG | delins | 1 | |||
| rs150934526 | 1.000 | 0.040 | 5 | 121330628 | intron variant | T/C | snv | 1.1E-02 | 1 | ||
| rs183819925 | 1.000 | 0.040 | 4 | 175138126 | intron variant | G/T | snv | 9.7E-03 | 1 | ||
| rs184148048 | 1.000 | 0.040 | 2 | 66212157 | intergenic variant | A/T | snv | 1.3E-02 | 1 | ||
| rs189010983 | 1.000 | 0.040 | 12 | 83692397 | intergenic variant | C/A;T | snv | 1.4E-02 | 1 | ||
| rs190797076 | 1.000 | 0.040 | 4 | 110589931 | intergenic variant | G/A;T | snv | 9.7E-03 | 1 | ||
| rs1955873 | 1.000 | 0.040 | 14 | 25573788 | intergenic variant | A/G | snv | 0.97 | 1 | ||
| rs201958930 | 1.000 | 0.040 | 4 | 58871307 | intron variant | AAA/-;AA;AAAA | delins | 1 | |||
| rs209345 | 1.000 | 0.040 | 5 | 162064381 | intron variant | T/C;G | snv | 1 | |||
| rs6092354 | 1.000 | 0.040 | 20 | 56719418 | intergenic variant | G/T | snv | 7.5E-02 | 1 | ||
| rs6708110 | 1.000 | 0.040 | 2 | 4007215 | intergenic variant | G/C | snv | 6.4E-02 | 1 | ||
| rs71370433 | 1.000 | 0.040 | 17 | 6294504 | intergenic variant | C/T | snv | 1.3E-02 | 1 | ||
| rs73078593 | 1.000 | 0.040 | 20 | 12310875 | intron variant | C/A | snv | 4.1E-02 | 1 | ||
| rs73126576 | 1.000 | 0.040 | 20 | 39961687 | regulatory region variant | T/C | snv | 2.9E-02 | 1 | ||
| rs73989024 | 1.000 | 0.040 | 17 | 49932105 | intron variant | A/G | snv | 5.5E-02 | 1 | ||
| rs74852193 | 1.000 | 0.040 | 1 | 68698339 | non coding transcript exon variant | G/A | snv | 3.8E-02 | 1 | ||
| rs76065397 | 1.000 | 0.040 | 15 | 35904724 | intergenic variant | T/C | snv | 1.8E-02 | 1 |