| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2278293 | 0.882 | 0.040 | 7 | 128400698 | non coding transcript exon variant | C/T | snv | 0.47 | 3 | ||
| rs7588571 | 0.882 | 0.040 | 2 | 79161461 | intron variant | G/A | snv | 0.49 | 3 | ||
| rs1238539471 | 1.000 | 0.040 | 16 | 50710637 | synonymous variant | A/G | snv | 7.0E-06 | 2 | ||
| rs1367967034 | 1.000 | 0.040 | 16 | 50707959 | splice region variant | A/G | snv | 4.0E-06 | 2 | ||
| rs17114808 | 0.925 | 0.040 | 10 | 102631528 | 3 prime UTR variant | C/A;G;T | snv | 2 | |||
| rs3092936 | 1.000 | 0.040 | X | 136654046 | intron variant | T/C | snv | 8.9E-02 | 2 | ||
| rs4833079 | 1.000 | 0.040 | 4 | 38653060 | intron variant | T/C | snv | 0.30 | 2 | ||
| rs6531656 | 1.000 | 0.040 | 4 | 38682580 | intron variant | C/T | snv | 0.87 | 2 | ||
| rs10737416 | 1.000 | 0.040 | 1 | 224887055 | intergenic variant | C/A;T | snv | 1 | |||
| rs17582214 | 1.000 | 0.040 | 9 | 119676531 | regulatory region variant | A/G;T | snv | 1 | |||
| rs2302217 | 1.000 | 0.040 | 19 | 498524 | synonymous variant | A/C;G | snv | 1.6E-05; 0.51 | 1 | ||
| rs2310241 | 1.000 | 0.040 | 2 | 102225489 | intron variant | A/C | snv | 0.44 | 1 | ||
| rs3004070 | 1.000 | 0.040 | 6 | 39902176 | 3 prime UTR variant | T/A | snv | 0.51 | 1 | ||
| rs337629 | 1.000 | 0.040 | 4 | 38633737 | intron variant | A/G;T | snv | 1 | |||
| rs4415345 | 1.000 | 0.040 | 8 | 7057895 | upstream gene variant | G/A;C | snv | 1 | |||
| rs4610776 | 1.000 | 0.040 | 8 | 7057155 | upstream gene variant | A/T | snv | 0.26 | 1 | ||
| rs4837656 | 1.000 | 0.040 | 9 | 119671775 | intergenic variant | T/C | snv | 0.27 | 1 | ||
| rs2278294 | 0.882 | 0.080 | 7 | 128400645 | non coding transcript exon variant | C/T | snv | 0.38 | 3 | ||
| rs4364254 | 0.882 | 0.080 | 4 | 83302560 | intron variant | C/T | snv | 0.63 | 3 | ||
| rs7251 | 0.925 | 0.080 | 19 | 49659652 | missense variant | C/A;G | snv | 0.39 | 0.44 | 2 | |
| rs6195 | 0.807 | 0.120 | 5 | 143399752 | missense variant | T/A;C | snv | 6 | |||
| rs37972 | 0.851 | 0.160 | 7 | 7967878 | 3 prime UTR variant | T/A;C | snv | 5 | |||
| rs4845618 | 0.851 | 0.160 | 1 | 154427539 | intron variant | G/T | snv | 0.53 | 5 | ||
| rs3092952 | 0.925 | 0.160 | X | 136644791 | upstream gene variant | A/G | snv | 0.29 | 3 | ||
| rs3092920 | 0.925 | 0.160 | X | 136661832 | downstream gene variant | G/T | snv | 0.23 | 2 |