| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9936170 | 1.000 | 0.040 | 16 | 87477955 | intron variant | A/C;G | snv | 1 | |||
| rs2349775 | 0.851 | 0.120 | 7 | 8678450 | intron variant | G/A;C | snv | 6 | |||
| rs78260322 | 1.000 | 0.040 | 2 | 86566075 | intron variant | A/G | snv | 7.4E-02 | 1 | ||
| rs9828595 | 1.000 | 0.040 | 3 | 85843897 | intron variant | T/A;C;G | snv | 1 | |||
| rs7355953 | 1.000 | 0.040 | 3 | 85742987 | intron variant | T/A;C | snv | 0.16 | 1 | ||
| rs9829032 | 0.925 | 0.080 | 3 | 85634450 | intron variant | A/G | snv | 0.41 | 2 | ||
| rs4856278 | 1.000 | 0.040 | 3 | 85599499 | intron variant | A/G;T | snv | 1 | |||
| rs6807666 | 1.000 | 0.040 | 3 | 85545278 | intron variant | A/C | snv | 0.59 | 1 | ||
| rs62250661 | 1.000 | 0.040 | 3 | 85402044 | intron variant | C/A | snv | 0.38 | 1 | ||
| rs9854869 | 1.000 | 0.040 | 3 | 85371574 | intron variant | C/A | snv | 0.17 | 2 | ||
| rs1368748 | 1.000 | 0.040 | 3 | 85363180 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs9861237 | 1.000 | 0.040 | 3 | 85353319 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs76508707 | 1.000 | 0.040 | 3 | 85347899 | intron variant | C/T | snv | 0.43 | 2 | ||
| rs62253085 | 1.000 | 0.040 | 3 | 85344618 | intron variant | A/G;T | snv | 1 | |||
| rs9811546 | 1.000 | 0.040 | 3 | 85342522 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs818219 | 1.000 | 0.040 | 3 | 85325439 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs9837462 | 1.000 | 0.040 | 3 | 85109415 | intron variant | C/A | snv | 0.25 | 1 | ||
| rs1248860 | 1.000 | 0.040 | 3 | 84966628 | intron variant | G/A | snv | 0.56 | 2 | ||
| rs9870384 | 1.000 | 0.040 | 3 | 84960666 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs56084168 | 1.000 | 0.040 | 17 | 81110774 | 3 prime UTR variant | C/T | snv | 0.15 | 1 | ||
| rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 43 | |
| rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 37 | |
| rs57875989 | 0.882 | 0.080 | 1 | 7829913 | splice acceptor variant | GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC | delins | 0.11 | 0.18 | 7 | |
| rs228697 | 0.882 | 0.080 | 1 | 7827519 | missense variant | C/G | snv | 8.7E-02 | 7.3E-02 | 5 | |
| rs61991614 | 1.000 | 0.040 | 14 | 77018366 | regulatory region variant | G/A | snv | 0.21 | 1 |