| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6446592 | 0.925 | 0.040 | 4 | 7340998 | intron variant | T/C | snv | 0.17 | 2 | ||
| rs4234795 | 1.000 | 0.080 | 4 | 7209075 | intron variant | A/C;G;T | snv | 1 | |||
| rs13125782 | 1.000 | 0.040 | 4 | 7426539 | intron variant | T/A;C;G | snv | 1 | |||
| rs4689803 | 1.000 | 0.040 | 4 | 7623930 | intron variant | T/A | snv | 0.77 | 1 | ||
| rs12642344 | 1.000 | 0.040 | 4 | 7623904 | intron variant | C/T | snv | 0.21 | 1 | ||
| rs10937844 | 1.000 | 0.040 | 4 | 7624252 | intron variant | C/A;T | snv | 1 | |||
| rs10002854 | 1.000 | 0.040 | 4 | 7519419 | intron variant | C/T | snv | 8.8E-02 | 1 | ||
| rs744355 | 1.000 | 0.040 | 4 | 7521637 | intron variant | T/C | snv | 0.35 | 1 | ||
| rs744356 | 1.000 | 0.040 | 4 | 7521546 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs6838261 | 1.000 | 0.040 | 4 | 7623685 | intron variant | T/C | snv | 0.31 | 1 | ||
| rs10470722 | 1.000 | 0.040 | 4 | 7516784 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs13114336 | 1.000 | 0.040 | 4 | 7517591 | intron variant | G/C | snv | 5.7E-02 | 1 | ||
| rs11731003 | 1.000 | 0.080 | 4 | 7388545 | intron variant | C/G;T | snv | 1 | |||
| rs4689642 | 1.000 | 0.040 | 4 | 7213595 | intron variant | A/G;T | snv | 1 | |||
| rs73214671 | 4 | 7570384 | intron variant | G/A | snv | 1.5E-02 | 1 | ||||
| rs111913416 | 4 | 7706148 | intron variant | A/T | snv | 0.19 | 1 | ||||
| rs35791045 | 4 | 7425380 | intron variant | A/G | snv | 0.11 | 1 | ||||
| rs10023470 | 4 | 7432729 | 3 prime UTR variant | A/G | snv | 0.20 | 1 | ||||
| rs77191210 | 4 | 7434974 | intron variant | C/T | snv | 0.16 | 1 |