| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs57374291 | 1.000 | 0.080 | 10 | 87933078 | missense variant | G/A;T | snv | 2 | |||
| rs586339 | 1.000 | 0.080 | 1 | 43671586 | missense variant | C/A;G;T | snv | 0.70 | 0.78 | 2 | |
| rs6601328 | 1.000 | 0.080 | 8 | 9545693 | regulatory region variant | G/A;C | snv | 2 | |||
| rs7015700 | 1.000 | 0.080 | 8 | 9670197 | splice donor variant | G/A | snv | 0.23 | 2 | ||
| rs7040869 | 1.000 | 0.080 | 9 | 99072866 | downstream gene variant | G/A | snv | 0.11 | 2 | ||
| rs7186128 | 1.000 | 0.080 | 16 | 16864058 | intergenic variant | G/A | snv | 0.70 | 2 | ||
| rs758222990 | 1.000 | 0.080 | 17 | 39725363 | missense variant | C/G;T | snv | 1.2E-05 | 2 | ||
| rs778199483 | 1.000 | 0.080 | 7 | 55181313 | missense variant | C/G;T | snv | 4.8E-05 | 2 | ||
| rs779179533 | 1.000 | 0.080 | 3 | 189808322 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs1001581 | 1.000 | 0.080 | 19 | 43561236 | intron variant | C/T | snv | 0.38 | 1 | ||
| rs10023113 | 1.000 | 0.080 | 4 | 113625548 | intron variant | A/G | snv | 0.18 | 1 | ||
| rs1005165 | 1.000 | 0.080 | 19 | 45405792 | intron variant | C/T | snv | 0.21 | 1 | ||
| rs1042852 | 1.000 | 0.080 | 3 | 105658671 | 3 prime UTR variant | C/G;T | snv | 1 | |||
| rs1057519858 | 1.000 | 0.080 | 19 | 1220495 | missense variant | G/T | snv | 1 | |||
| rs1059292 | 1.000 | 0.080 | 11 | 62855579 | non coding transcript exon variant | T/C | snv | 7.2E-02 | 9.0E-02 | 1 | |
| rs1077424 | 1.000 | 0.080 | 1 | 57344632 | intron variant | G/C | snv | 0.52 | 1 | ||
| rs10878232 | 1.000 | 0.080 | 12 | 65128867 | intergenic variant | T/A;C;G | snv | 1 | |||
| rs10981694 | 1.000 | 0.080 | 9 | 113224129 | intron variant | T/G | snv | 8.7E-02 | 1 | ||
| rs11045585 | 1.000 | 0.080 | 12 | 20892760 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs11071938 | 1.000 | 0.080 | 15 | 67127649 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs11080466 | 1.000 | 0.080 | 18 | 10899030 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs11207010 | 1.000 | 0.080 | 1 | 57337214 | intron variant | G/C | snv | 0.41 | 1 | ||
| rs11574852 | 1.000 | 0.080 | 10 | 102401718 | intron variant | A/C | snv | 2.3E-02 | 2.3E-02 | 1 | |
| rs11674251 | 1.000 | 0.080 | 2 | 20016748 | upstream gene variant | T/C | snv | 0.18 | 1 | ||
| rs11713419 | 1.000 | 0.080 | 3 | 3108583 | 5 prime UTR variant | A/G | snv | 0.19 | 1 |