| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
| rs1800440 | 0.653 | 0.440 | 2 | 38070996 | missense variant | T/C;G | snv | 0.15; 4.0E-06 | 6 | ||
| rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 5 | ||
| rs11375254 | 0.882 | 0.080 | 3 | 189625454 | intergenic variant | A/-;AA;AAA;AAAA | delins | 3 | |||
| rs217727 | 0.641 | 0.480 | 11 | 1995678 | non coding transcript exon variant | G/A | snv | 0.20 | 3 | ||
| rs31490 | 0.776 | 0.280 | 5 | 1344343 | splice region variant | G/A;T | snv | 0.37; 8.0E-06 | 3 | ||
| rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 3 | ||
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
| rs2018683 | 1.000 | 0.080 | 7 | 28974579 | intergenic variant | G/A;T | snv | 2 | |||
| rs2293607 | 0.807 | 0.200 | 3 | 169764547 | non coding transcript exon variant | T/A;C | snv | 2 | |||
| rs4236709 | 0.925 | 0.080 | 8 | 32552592 | intron variant | G/A;T | snv | 2 | |||
| rs4588 | 0.597 | 0.720 | 4 | 71752606 | missense variant | G/A;T | snv | 1.6E-05; 0.25 | 2 | ||
| rs6495309 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 2 | |||
| rs12051272 | 0.925 | 0.120 | 16 | 82629683 | intron variant | G/C;T | snv | 1 | |||
| rs12265047 | 1.000 | 0.080 | 10 | 112728166 | intron variant | G/A;C | snv | 1 | |||
| rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 1 | ||
| rs1800449 | 0.641 | 0.400 | 5 | 122077513 | missense variant | C/A;T | snv | 4.0E-06; 0.17 | 1 | ||
| rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 1 | ||
| rs1853837 | 1.000 | 0.080 | 6 | 41529297 | intron variant | C/A;T | snv | 1 | |||
| rs2279574 | 0.827 | 0.120 | 12 | 89351700 | missense variant | C/A;T | snv | 0.52 | 1 | ||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 1 | ||
| rs9657904 | 0.925 | 0.160 | 3 | 105867870 | intron variant | T/A;C | snv | 1 | |||
| rs17635492 | 1.000 | 0.080 | 6 | 117450114 | intron variant | A/T | snv | 2.4E-02 | 2 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 6 | |
| rs16950650 | 1.000 | 0.080 | 13 | 95123178 | intron variant | C/T | snv | 4.7E-02 | 2 |