| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs756706958 | 0.925 | 0.080 | 7 | 140776967 | missense variant | T/C | snv | 2 | |||
| rs1131692058 | 1.000 | 0.080 | 7 | 140734769 | splice acceptor variant | TCTACA/- | delins | 1 | |||
| rs1267636 | 1.000 | 0.080 | 7 | 140792239 | intron variant | T/C | snv | 0.11 | 1 | ||
| rs1370423184 | 1.000 | 0.080 | 7 | 140778018 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
| rs17161747 | 1.000 | 0.080 | 7 | 140858940 | intron variant | G/C | snv | 5.5E-02 | 1 | ||
| rs17623204 | 1.000 | 0.080 | 7 | 140806604 | intron variant | T/A | snv | 5.5E-02 | 1 | ||
| rs180177032 | 1.000 | 0.080 | 7 | 140781623 | missense variant | C/A | snv | 1 | |||
| rs180177033 | 1.000 | 0.080 | 7 | 140781620 | missense variant | A/C | snv | 1 | |||
| rs35407685 | 1.000 | 0.080 | 7 | 140786444 | intron variant | -/G | delins | 1 | |||
| rs397516890 | 1.000 | 0.080 | 7 | 140781601 | inframe deletion | TCC/- | del | 1 | |||
| rs397516897 | 1.000 | 0.080 | 7 | 140753334 | inframe deletion | TCA/- | del | 1 | |||
| rs6464149 | 1.000 | 0.080 | 7 | 140926036 | upstream gene variant | A/C | snv | 0.12 | 1 | ||
| rs7810757 | 1.000 | 0.080 | 7 | 140925302 | upstream gene variant | T/C | snv | 0.15 | 1 | ||
| rs9648716 | 1.000 | 0.080 | 7 | 140912363 | intron variant | A/G;T | snv | 0.31 | 1 | ||
| rs3748093 | 0.925 | 0.120 | 7 | 140800651 | intron variant | T/A | snv | 1.5E-02 | 4 | ||
| rs121913340 | 1.000 | 0.120 | 7 | 140753379 | missense variant | C/T | snv | 1 | |||
| rs180177039 | 0.851 | 0.160 | 7 | 140778006 | missense variant | T/A;C;G | snv | 12 | |||
| rs1225976306 | 0.807 | 0.160 | 7 | 140924673 | missense variant | C/T | snv | 9.3E-06 | 8 | ||
| rs869025340 | 0.925 | 0.160 | 7 | 140777032 | missense variant | A/C;G;T | snv | 5 | |||
| rs121913353 | 0.925 | 0.160 | 7 | 140781612 | missense variant | C/G;T | snv | 3 | |||
| rs397516893 | 0.925 | 0.160 | 7 | 140778048 | missense variant | A/C | snv | 3 | |||
| rs1057519718 | 0.925 | 0.160 | 7 | 140753355 | missense variant | CA/TC | mnv | 2 | |||
| rs397507477 | 1.000 | 0.160 | 7 | 140777995 | missense variant | G/A | snv | 2 | |||
| rs606231228 | 0.925 | 0.160 | 7 | 140777013 | missense variant | C/A;G | snv | 2 | |||
| rs180177037 | 1.000 | 0.160 | 7 | 140778013 | missense variant | T/C | snv | 1 |