| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3128965 | 0.882 | 0.280 | 6 | 33088122 | 3 prime UTR variant | G/A | snv | 0.14 | 1 | ||
| rs3790566 | 1.000 | 0.040 | 1 | 67348757 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs6659932 | 0.827 | 0.240 | 1 | 67336688 | intron variant | A/C | snv | 0.81 | 1 | ||
| rs12722495 | 0.851 | 0.200 | 10 | 6055320 | intron variant | T/C | snv | 7.0E-02 | 1 | ||
| rs1143679 | 0.732 | 0.520 | 16 | 31265490 | missense variant | G/A | snv | 9.7E-02 | 0.11 | 1 | |
| rs2359661 | 1.000 | 0.040 | 16 | 31269826 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs7190018 | 1.000 | 0.040 | 16 | 31290157 | intron variant | G/A;C | snv | 1 | |||
| rs2275247 | 0.925 | 0.080 | 1 | 35442850 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs4941246 | 1.000 | 0.040 | 18 | 64135070 | intron variant | C/T | snv | 0.60 | 1 | ||
| rs10220668 | 1.000 | 0.040 | 14 | 59042487 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs1857066 | 1.000 | 0.040 | 1 | 173363490 | non coding transcript exon variant | A/C | snv | 0.79 | 1 | ||
| rs117026326 | 0.752 | 0.440 | 7 | 74711703 | intron variant | C/T | snv | 1.3E-02 | 1 | ||
| rs3104398 | 1.000 | 0.040 | 6 | 32717908 | upstream gene variant | G/A | snv | 0.12 | 1 | ||
| rs3093024 | 0.882 | 0.200 | 6 | 167119305 | non coding transcript exon variant | A/G | snv | 0.61 | 1 | ||
| rs7900522 | 1.000 | 0.040 | 10 | 76350213 | intron variant | T/A;C | snv | 1 | |||
| rs6793295 | 0.827 | 0.240 | 3 | 169800667 | missense variant | T/C;G | snv | 0.37; 1.8E-04 | 1 | ||
| rs7665090 | 0.807 | 0.280 | 4 | 102630446 | downstream gene variant | A/G | snv | 0.55 | 1 | ||
| rs3918242 | 0.602 | 0.680 | 20 | 46007337 | upstream gene variant | C/T | snv | 0.14 | 1 | ||
| rs7934606 | 1.000 | 0.040 | 11 | 1100037 | intron variant | C/G;T | snv | 1 | |||
| rs564732150 | 1.000 | 0.040 | 6 | 31028355 | missense variant | C/T | snv | 1 | |||
| rs936469 | 1.000 | 0.040 | 11 | 606749 | non coding transcript exon variant | G/A | snv | 0.24 | 1 | ||
| rs1372072 | 0.851 | 0.200 | 3 | 16913767 | intron variant | G/A | snv | 0.35 | 1 | ||
| rs2841277 | 0.882 | 0.120 | 14 | 104924668 | upstream gene variant | C/T | snv | 0.41 | 1 | ||
| rs3130573 | 1.000 | 0.040 | 6 | 31138491 | non coding transcript exon variant | A/C;G | snv | 8.1E-06; 0.33 | 1 | ||
| rs2176082 | 0.925 | 0.080 | 3 | 58345459 | intron variant | G/A | snv | 0.36 | 1 |