| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs600491 | 0.925 | 0.080 | 1 | 54867852 | intron variant | C/A;T | snv | 2 | |||
| rs119475041 | 1.000 | 0.080 | 1 | 54875134 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs281797256 | 1.000 | 0.080 | 1 | 54865405 | missense variant | C/G | snv | 1 | |||
| rs281797257 | 1.000 | 0.080 | 1 | 54865442 | missense variant | T/G | snv | 1 | |||
| rs28939092 | 1.000 | 0.080 | 1 | 54852372 | missense variant | T/G | snv | 4.0E-06 | 1 | ||
| rs387906938 | 1.000 | 0.080 | 1 | 54883698 | missense variant | G/A | snv | 1 | |||
| rs387906939 | 1.000 | 0.080 | 1 | 54883724 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs387906940 | 1.000 | 0.080 | 1 | 54852346 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs597021 | 1 | 54873765 | intron variant | G/T | snv | 0.62 | 1 | ||||
| rs638944 | 1.000 | 0.080 | 1 | 54876242 | intron variant | T/G | snv | 0.51 | 1 | ||
| rs718265 | 1.000 | 0.080 | 1 | 54854229 | synonymous variant | A/G | snv | 0.66 | 0.67 | 1 | |
| rs7374 | 1.000 | 0.080 | 1 | 54850649 | 3 prime UTR variant | A/G | snv | 0.40 | 1 |