| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 12 | |
| rs1160985 | 1.000 | 0.080 | 19 | 44900155 | intron variant | C/T | snv | 0.52 | 5 | ||
| rs157582 | 0.851 | 0.160 | 19 | 44892962 | intron variant | C/T | snv | 0.24 | 0.29 | 5 | |
| rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 4 | ||
| rs8106922 | 1.000 | 0.080 | 19 | 44898409 | intron variant | A/G | snv | 0.36 | 3 | ||
| rs1038026 | 1.000 | 0.080 | 19 | 44901805 | 3 prime UTR variant | A/G;T | snv | 3 | |||
| rs77301115 | 1.000 | 0.080 | 19 | 44893716 | intron variant | G/A | snv | 2.8E-02 | 2 | ||
| rs157588 | 19 | 44895007 | intron variant | C/T | snv | 0.59 | 2 | ||||
| rs61679753 | 1.000 | 0.080 | 19 | 44897490 | intron variant | T/A | snv | 5.6E-02 | 1 | ||
| rs142412517 | 1.000 | 0.080 | 19 | 44900801 | missense variant | C/T | snv | 4.9E-04 | 5.7E-04 | 1 | |
| rs35568738 | 1.000 | 0.080 | 19 | 44899461 | intron variant | G/A;C | snv | 1 | |||
| rs117310449 | 1.000 | 0.080 | 19 | 44890259 | intron variant | C/T | snv | 7.3E-03 | 1 | ||
| rs1160984 | 1.000 | 0.080 | 19 | 44900667 | intron variant | C/T | snv | 3.9E-02 | 1 | ||
| rs394819 | 1.000 | 0.080 | 19 | 44901322 | missense variant | G/A;T | snv | 3.7E-05; 9.7E-03 | 1 | ||
| rs59007384 | 0.851 | 0.080 | 19 | 44893408 | intron variant | G/A;T | snv | 1 | |||
| rs141864196 | 1.000 | 0.080 | 19 | 44902242 | 3 prime UTR variant | G/A | snv | 1.7E-02 | 1 | ||
| rs11668327 | 1.000 | 0.080 | 19 | 44895376 | intron variant | G/C | snv | 0.12 | 1 | ||
| rs561654715 | 1.000 | 0.080 | 19 | 44890947 | intron variant | G/A | snv | 1.7E-03 | 1 | ||
| rs76692773 | 1.000 | 0.080 | 19 | 44890954 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
| rs71352238 | 1.000 | 0.080 | 19 | 44891079 | intron variant | T/C | snv | 0.10 | 1 | ||
| rs405697 | 1.000 | 0.080 | 19 | 44901434 | 3 prime UTR variant | A/G;T | snv | 1 | |||
| rs760136 | 1.000 | 0.080 | 19 | 44900601 | intron variant | A/G | snv | 0.52 | 1 | ||
| rs10119 | 0.925 | 0.080 | 19 | 44903416 | 3 prime UTR variant | G/A | snv | 0.28 | 1 | ||
| rs115881343 | 1.000 | 0.040 | 19 | 44899959 | intron variant | C/G;T | snv | 2.9E-02 | 1 |