| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5745908 | 1.000 | 0.200 | 15 | 75349341 | splice donor variant | T/C | snv | 7.2E-03 | 6.9E-03 | 1 | |
| rs2075818 | 1.000 | 0.200 | 7 | 30456766 | synonymous variant | G/A;C;T | snv | 1.6E-05; 0.28 | 1 | ||
| rs746055479 | 1.000 | 0.200 | 16 | 50712108 | missense variant | G/A;T | snv | 2.4E-05 | 1 | ||
| rs752615209 | 1.000 | 0.200 | 16 | 50710956 | missense variant | C/G;T | snv | 8.0E-06 | 1 | ||
| rs886040969 | 1.000 | 0.200 | 16 | 50712357 | missense variant | G/A | snv | 1 | |||
| rs9316059 | 1.000 | 0.200 | 13 | 43912653 | intron variant | A/C;T | snv | 1 | |||
| rs1462891 | 1.000 | 0.200 | 8 | 31973417 | intron variant | T/C | snv | 0.72 | 1 | ||
| rs383632 | 1.000 | 0.200 | 8 | 31948532 | intron variant | T/C;G | snv | 1 | |||
| rs7854303 | 1.000 | 0.200 | 9 | 5557672 | missense variant | T/C | snv | 1.00 | 1.00 | 1 | |
| rs17633132 | 1.000 | 0.200 | 8 | 17642610 | splice region variant | C/G;T | snv | 8.0E-06; 0.11 | 1 | ||
| rs4857037 | 1.000 | 0.200 | 3 | 93908968 | intron variant | G/A | snv | 0.89 | 1 | ||
| rs3095324 | 1.000 | 0.200 | 6 | 31119356 | intron variant | C/T | snv | 0.35 | 1 | ||
| rs774164456 | 1.000 | 0.200 | 15 | 77032888 | missense variant | G/A;C | snv | 2.6E-05 | 1 | ||
| rs111874856 | 1.000 | 0.200 | 18 | 21028924 | missense variant | C/T | snv | 1 | |||
| rs112108028 | 1.000 | 0.200 | 18 | 20959861 | missense variant | G/A | snv | 1 | |||
| rs112130712 | 1.000 | 0.200 | 18 | 20967783 | missense variant | T/C | snv | 1 | |||
| rs2834643 | 1.000 | 0.200 | 21 | 34814099 | intron variant | A/G | snv | 0.42 | 1 | ||
| rs7572482 | 1.000 | 0.200 | 2 | 191150346 | intron variant | A/C;G | snv | 1 | |||
| rs7574070 | 1.000 | 0.200 | 2 | 191145762 | intron variant | A/C | snv | 0.55 | 1 | ||
| rs2061634 | 1.000 | 0.200 | 9 | 97343500 | missense variant | C/G | snv | 0.27 | 0.30 | 1 | |
| rs17006292 | 1.000 | 0.200 | 2 | 121261187 | intron variant | C/A | snv | 2.8E-02 | 1 | ||
| rs370893734 | 1.000 | 0.200 | 6 | 31577481 | missense variant | G/A;T | snv | 2.0E-05; 1.6E-05 | 1 | ||
| rs886039866 | 1.000 | 0.200 | 12 | 6333376 | missense variant | G/A | snv | 1 | |||
| rs3789205 | 1.000 | 0.200 | 6 | 41286177 | intron variant | A/G | snv | 9.4E-02 | 1 | ||
| rs7999348 | 1.000 | 0.200 | 13 | 99280668 | intron variant | G/A;C | snv | 1 |