| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs999947969 | 0.827 | 0.080 | 7 | 80671145 | synonymous variant | C/T | snv | 7 | |||
| rs9985766 | 1.000 | 0.040 | 4 | 150108918 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs9982601 | 0.851 | 0.080 | 21 | 34226827 | intron variant | C/T | snv | 0.15 | 4 | ||
| rs9978142 | 1.000 | 0.040 | 21 | 34279939 | intron variant | A/G;T | snv | 0.15 | 4 | ||
| rs9972711 | 1.000 | 0.040 | 16 | 15808733 | intron variant | A/G;T | snv | 1 | |||
| rs997251 | 1.000 | 0.040 | 1 | 85379684 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs9970807 | 0.925 | 0.080 | 1 | 56499992 | intron variant | C/T | snv | 0.11 | 2 | ||
| rs9964304 | 1.000 | 0.040 | 18 | 49703347 | intergenic variant | A/C | snv | 0.33 | 1 | ||
| rs9949 | 1.000 | 0.040 | 8 | 9137002 | 3 prime UTR variant | A/G;T | snv | 1 | |||
| rs9943582 | 0.807 | 0.120 | 11 | 57237593 | upstream gene variant | T/C | snv | 0.63 | 8 | ||
| rs993969 | 1.000 | 0.040 | 4 | 189704840 | upstream gene variant | A/T | snv | 1 | |||
| rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
| rs9912587 | 1.000 | 0.040 | 17 | 43021069 | intron variant | G/A | snv | 0.28 | 1 | ||
| rs9902941 | 1.000 | 0.040 | 17 | 17830446 | intron variant | C/T | snv | 0.56 | 1 | ||
| rs9892152 | 1.000 | 0.040 | 17 | 64324605 | intron variant | T/C | snv | 0.49 | 1 | ||
| rs987401919 | 1.000 | 0.040 | 5 | 158690931 | downstream gene variant | C/T | snv | 2.1E-05 | 1 | ||
| rs9818870 | 0.807 | 0.200 | 3 | 138403280 | 3 prime UTR variant | C/A;T | snv | 9 | |||
| rs9804922 | 1.000 | 0.040 | 12 | 103519664 | intron variant | C/T | snv | 9.5E-02 | 1 | ||
| rs9797861 | 0.790 | 0.200 | 19 | 10632450 | intron variant | C/A;G;T | snv | 9 | |||
| rs978906 | 0.925 | 0.080 | 2 | 11183150 | 3 prime UTR variant | T/A;C | snv | 3 | |||
| rs9770242 | 0.851 | 0.240 | 7 | 106285885 | 5 prime UTR variant | C/A | snv | 0.79 | 5 | ||
| rs975722 | 1.000 | 0.040 | 7 | 117692860 | intron variant | A/G | snv | 0.53 | 1 | ||
| rs974819 | 0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv | 6 | |||
| rs972655070 | 0.882 | 0.040 | 1 | 161040282 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs965652 | 1.000 | 0.040 | 6 | 134047815 | intron variant | G/A | snv | 0.41 | 1 |