| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1000579 | 1.000 | 0.080 | 4 | 4717767 | intron variant | A/G | snv | 0.44 | 3 | ||
| rs10196867 | 0.925 | 0.080 | 2 | 79751234 | intron variant | C/G;T | snv | 5 | |||
| rs10198241 | 0.925 | 0.080 | 2 | 226115660 | intergenic variant | T/C | snv | 0.58 | 4 | ||
| rs10211296 | 1.000 | 0.080 | 2 | 165633833 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 1 | |||
| rs10392 | 0.882 | 0.160 | 20 | 38922292 | 3 prime UTR variant | G/A | snv | 0.17 | 6 | ||
| rs10483038 | 1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 | 3 | ||
| rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 1 | ||
| rs1057302 | 1.000 | 0.080 | 1 | 175157287 | 3 prime UTR variant | A/G | snv | 0.38 | 1 | ||
| rs10913569 | 1.000 | 0.080 | 1 | 178548873 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 5 | ||
| 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 | ||
| rs115357105 | 0.925 | 0.080 | 9 | 104376689 | intergenic variant | A/G | snv | 1.5E-02 | 4 | ||
| 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 | ||
| rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 1 | |
| rs11583322 | 1.000 | 0.080 | 1 | 36356711 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs11623335 | 1.000 | 0.080 | 14 | 56566358 | intron variant | G/A | snv | 0.85 | 1 | ||
| rs11681792 | 1.000 | 0.080 | 2 | 49957256 | intron variant | C/T | snv | 0.12 | 4 | ||
| rs11825659 | 0.925 | 0.080 | 11 | 133925624 | intron variant | A/G | snv | 0.12 | 4 | ||
| rs11922615 | 1.000 | 0.080 | 3 | 9416623 | intron variant | A/G | snv | 8.4E-02 | 1 | ||
| rs12006002 | 1.000 | 0.080 | 9 | 18166901 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs12180309 | 0.925 | 0.080 | 6 | 91209048 | intergenic variant | C/T | snv | 1.9E-02 | 4 |