| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11681792 | 1.000 | 0.080 | 2 | 49957256 | intron variant | C/T | snv | 0.12 | 4 | ||
| rs17028615 | 1.000 | 0.080 | 4 | 99150767 | intron variant | A/C;G | snv | 4 | |||
| rs1789882 | 1.000 | 0.080 | 4 | 99313896 | synonymous variant | A/G;T | snv | 0.82 | 4 | ||
| rs1789891 | 1.000 | 0.080 | 4 | 99329262 | intron variant | C/A | snv | 0.13 | 4 | ||
| rs279826 | 1.000 | 0.080 | 4 | 46332192 | intron variant | A/G | snv | 0.46 | 4 | ||
| rs34997829 | 1.000 | 0.080 | 10 | 124546821 | intron variant | G/C | snv | 0.24 | 4 | ||
| rs3743832 | 1.000 | 0.080 | 16 | 9120023 | 3 prime UTR variant | A/C | snv | 0.55 | 4 | ||
| rs1000579 | 1.000 | 0.080 | 4 | 4717767 | intron variant | A/G | snv | 0.44 | 3 | ||
| rs10211296 | 1.000 | 0.080 | 2 | 165633833 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs10483038 | 1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 | 3 | ||
| rs11075992 | 1.000 | 0.080 | 16 | 53786154 | intron variant | T/C | snv | 0.41 | 3 | ||
| rs111372083 | 1.000 | 0.080 | 21 | 37638374 | intron variant | C/A;T | snv | 0.27 | 3 | ||
| rs111576572 | 1.000 | 0.080 | 21 | 37617262 | 3 prime UTR variant | A/G | snv | 0.32 | 3 | ||
| rs1154433 | 1.000 | 0.080 | 4 | 99332551 | intron variant | A/G;T | snv | 3 | |||
| rs115460205 | 1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
| rs12482570 | 1.000 | 0.080 | 21 | 37705475 | intron variant | A/G | snv | 0.30 | 3 | ||
| rs12639833 | 1.000 | 0.080 | 4 | 99346215 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs12898370 | 1.000 | 0.080 | 15 | 77516256 | intergenic variant | A/C;T | snv | 3 | |||
| rs1316543 | 1.000 | 0.080 | 10 | 119445148 | intron variant | G/A | snv | 0.15 | 3 | ||
| rs1399590 | 1.000 | 0.080 | 21 | 37681768 | intron variant | G/A | snv | 0.56 | 3 | ||
| rs1399591 | 1.000 | 0.080 | 21 | 37681654 | intron variant | C/T | snv | 0.50 | 3 | ||
| rs1399592 | 1.000 | 0.080 | 21 | 37681559 | intron variant | T/A;G | snv | 0.52 | 3 | ||
| rs141424017 | 1.000 | 0.080 | 7 | 115311376 | intergenic variant | -/CAA | ins | 3 | |||
| rs1437396 | 1.000 | 0.080 | 2 | 55278320 | upstream gene variant | C/G;T | snv | 3 | |||
| rs143894582 | 1.000 | 0.080 | 12 | 112469070 | intron variant | A/-;AA | delins | 3 |