| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12670798 | 1.000 | 0.040 | 7 | 21567734 | intron variant | T/C | snv | 0.26 | 5 | ||
| rs12946454 | 0.925 | 0.040 | 17 | 45130754 | intron variant | A/T | snv | 0.21 | 5 | ||
| rs1384889210 | 0.827 | 0.040 | 11 | 116836193 | missense variant | C/A | snv | 5 | |||
| rs1501908 | 1.000 | 0.040 | 5 | 156971158 | intergenic variant | G/A;C;T | snv | 5 | |||
| rs17475879 | 0.925 | 0.040 | 6 | 30396731 | regulatory region variant | C/T | snv | 5.6E-02 | 5 | ||
| rs2298566 | 0.827 | 0.040 | 11 | 130880747 | missense variant | A/C;T | snv | 0.77; 4.0E-06 | 5 | ||
| rs2384550 | 1.000 | 0.040 | 12 | 114914926 | regulatory region variant | G/A | snv | 0.33 | 5 | ||
| rs448378 | 1.000 | 0.040 | 3 | 169383111 | intron variant | G/A;C | snv | 5 | |||
| rs4939883 | 1.000 | 0.040 | 18 | 49640844 | TF binding site variant | T/C;G | snv | 5 | |||
| rs6544713 | 0.925 | 0.040 | 2 | 43846742 | non coding transcript exon variant | T/C | snv | 0.75 | 5 | ||
| rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 5 | ||
| rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
| rs9332978 | 0.882 | 0.040 | 1 | 46942278 | upstream gene variant | T/C | snv | 7.3E-02 | 5 | ||
| rs1058930 | 0.882 | 0.040 | 10 | 95058362 | missense variant | G/A;C | snv | 1.0E-04; 3.7E-02 | 4 | ||
| rs116092985 | 0.882 | 0.040 | 16 | 2110972 | missense variant | A/G | snv | 6.5E-02 | 7.8E-02 | 4 | |
| rs1199475313 | 0.851 | 0.040 | 8 | 37966277 | missense variant | T/C | snv | 7.0E-06 | 4 | ||
| rs13144478 | 0.882 | 0.040 | 4 | 115275150 | regulatory region variant | A/T | snv | 5.5E-02 | 4 | ||
| rs142677199 | 0.882 | 0.040 | 17 | 63479897 | missense variant | G/A;T | snv | 3.2E-05 | 4 | ||
| rs16982520 | 1.000 | 0.040 | 20 | 59183665 | intron variant | A/G | snv | 0.14 | 4 | ||
| rs1790349 | 0.882 | 0.040 | 11 | 71431304 | intron variant | T/C | snv | 0.19 | 4 | ||
| rs180070 | 0.882 | 0.040 | 17 | 69960745 | upstream gene variant | G/T | snv | 0.77 | 4 | ||
| rs2015086 | 0.882 | 0.040 | 17 | 36064257 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
| rs255052 | 0.925 | 0.040 | 16 | 67991092 | intron variant | G/A | snv | 0.17 | 0.17 | 4 | |
| rs2967605 | 0.925 | 0.040 | 19 | 8404854 | downstream gene variant | C/T | snv | 0.20 | 4 | ||
| rs3736234 | 0.851 | 0.040 | 12 | 10160535 | non coding transcript exon variant | G/A | snv | 0.40 | 4 |