| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2333227 | 0.752 | 0.320 | 17 | 58281401 | upstream gene variant | C/T | snv | 0.24 | 15 | ||
| rs56378716 | 1.000 | 0.080 | 17 | 58279141 | missense variant | A/G | snv | 1.0E-02 | 9.8E-03 | 6 | |
| rs34097845 | 1.000 | 0.080 | 17 | 58281068 | upstream gene variant | C/T | snv | 4.3E-02 | 4 | ||
| rs7208693 | 0.882 | 0.080 | 17 | 58280457 | missense variant | C/A;T | snv | 9.0E-02 | 4 | ||
| rs1207692596 | 0.925 | 0.080 | 17 | 58280438 | missense variant | G/A;T | snv | 3 | |||
| rs35897051 | 1.000 | 0.080 | 17 | 58270865 | splice acceptor variant | T/G | snv | 4.4E-03 | 4.6E-03 | 3 | |
| rs376373278 | 0.882 | 0.120 | 17 | 58279015 | missense variant | G/A;C | snv | 4.2E-06 | 3 | ||
| rs972427414 | 0.882 | 0.120 | 17 | 58279379 | missense variant | A/G | snv | 3 | |||
| rs1271546630 | 1.000 | 0.120 | 17 | 58277848 | missense variant | G/A;C | snv | 2 | |||
| rs2107545 | 0.925 | 0.160 | 17 | 58282757 | upstream gene variant | A/G | snv | 0.28 | 2 | ||
| rs2243828 | 0.925 | 0.080 | 17 | 58281523 | upstream gene variant | A/G;T | snv | 2 | |||
| rs28730837 | 1.000 | 0.080 | 17 | 58278036 | missense variant | G/A | snv | 1.2E-02 | 1.2E-02 | 2 | |
| rs767523236 | 0.925 | 0.040 | 17 | 58279033 | missense variant | T/C | snv | 4.1E-06 | 7.0E-06 | 2 | |
| rs8082134 | 0.925 | 0.080 | 17 | 58275265 | intron variant | G/A;T | snv | 2 | |||
| rs119468010 | 1.000 | 0.080 | 17 | 58272835 | missense variant | G/A | snv | 1.5E-03 | 1.7E-03 | 1 | |
| rs119469012 | 1.000 | 0.080 | 17 | 58272825 | missense variant | A/C;G | snv | 1 | |||
| rs119469013 | 1.000 | 0.080 | 17 | 58273534 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs119469014 | 1.000 | 0.080 | 17 | 58273540 | missense variant | G/A;C | snv | 2.4E-05; 2.0E-05 | 1 | ||
| rs1195782955 | 1.000 | 0.040 | 17 | 58279411 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1351260902 | 1.000 | 0.080 | 17 | 58279839 | missense variant | C/G;T | snv | 1 | |||
| rs376919235 | 1.000 | 0.080 | 17 | 58279366 | synonymous variant | A/G | snv | 1.4E-05 | 7.0E-06 | 1 | |
| rs536522394 | 1.000 | 0.080 | 17 | 58273467 | frameshift variant | TTGGGTTCCATGGG/-;TTGGGTTCCATGGGTTGGGTTCCATGGG | delins | 8.3E-04 | 1 | ||
| rs759684602 | 1.000 | 0.080 | 17 | 58279136 | missense variant | T/C | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs762688992 | 1.000 | 0.080 | 17 | 58275567 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
| rs78950939 | 1.000 | 0.080 | 17 | 58279553 | missense variant | T/C | snv | 4.6E-04 | 5.0E-04 | 1 |