| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3789604 | 0.776 | 0.360 | 1 | 113812320 | synonymous variant | T/A;C;G | snv | 8.5E-06; 1.3E-05; 0.17 | 9 | ||
| rs2153977 | 0.807 | 0.240 | 1 | 113537449 | intron variant | C/T | snv | 0.28 | 6 | ||
| rs2746071 | 0.882 | 0.160 | 1 | 192808434 | intron variant | A/G | snv | 0.35 | 4 | ||
| rs7533564 | 0.925 | 0.120 | 1 | 78360228 | intron variant | C/T | snv | 0.92 | 4 | ||
| rs12566340 | 0.925 | 0.200 | 1 | 113877706 | 3 prime UTR variant | C/A;T | snv | 3 | |||
| rs10914542 | 0.925 | 0.120 | 1 | 32262639 | intron variant | C/G | snv | 0.15 | 2 | ||
| rs10918706 | 0.925 | 0.200 | 1 | 167496884 | intron variant | C/T | snv | 0.24 | 2 | ||
| rs1214611 | 0.925 | 0.200 | 1 | 167479867 | intron variant | A/G | snv | 0.54 | 2 | ||
| rs2269241 | 1.000 | 0.120 | 1 | 63643100 | intron variant | T/C | snv | 0.23 | 2 | ||
| rs2358994 | 0.925 | 0.120 | 1 | 113886839 | intron variant | G/A | snv | 0.16 | 2 | ||
| rs3820589 | 0.925 | 0.200 | 1 | 42960373 | intron variant | A/T | snv | 8.3E-02 | 2 | ||
| rs559047 | 1.000 | 0.120 | 1 | 238590616 | intergenic variant | T/A;C | snv | 2 | |||
| rs1217385 | 1.000 | 0.120 | 1 | 113875583 | intron variant | A/C | snv | 0.58 | 1 | ||
| rs1217412 | 1.000 | 0.120 | 1 | 113814589 | 3 prime UTR variant | G/A | snv | 0.78 | 1 | ||
| rs1217419 | 1.000 | 0.120 | 1 | 113859282 | intron variant | T/G | snv | 0.56 | 1 | ||
| rs1450261764 | 1.000 | 0.120 | 1 | 113856592 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
| rs2949655 | 1.000 | 0.120 | 1 | 167482613 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs56048322 | 1.000 | 0.120 | 1 | 113829592 | missense variant | C/G | snv | 5.8E-03 | 5.9E-03 | 1 | |
| rs6691977 | 1.000 | 0.120 | 1 | 200845831 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs672797 | 1.000 | 0.120 | 1 | 81094869 | downstream gene variant | C/A;T | snv | 0.63 | 1 | ||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
| rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
| rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 44 | ||
| rs1800587 | 0.620 | 0.720 | 2 | 112785383 | upstream gene variant | G/A;C | snv | 0.32 | 43 |