| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12568784 | 0.925 | 0.120 | 1 | 152350656 | stop gained | G/A;T | snv | 0.24 | 0.21 | 2 | |
| rs1443712053 | 0.925 | 0.120 | 1 | 152310672 | stop gained | G/C | snv | 4.0E-06 | 2 | ||
| rs145627745 | 0.925 | 0.120 | 1 | 152313145 | missense variant | T/A | snv | 7.8E-03 | 8.0E-03 | 2 | |
| rs16833974 | 0.925 | 0.120 | 1 | 152354040 | missense variant | T/C | snv | 1.6E-02 | 6.1E-02 | 2 | |
| rs180768115 | 0.925 | 0.120 | 1 | 152310342 | stop gained | G/C;T | snv | 8.0E-06; 1.7E-04 | 2 | ||
| rs2066446 | 0.925 | 0.120 | 1 | 67315434 | intron variant | A/G | snv | 0.20 | 2 | ||
| rs28441202 | 0.925 | 0.120 | 1 | 152156387 | missense variant | A/G | snv | 2 | |||
| rs4363385 | 0.925 | 0.120 | 1 | 153016845 | upstream gene variant | T/C | snv | 0.62 | 2 | ||
| rs560912365 | 0.925 | 0.120 | 1 | 152309046 | stop gained | C/G;T | snv | 4.0E-06; 2.2E-04 | 2 | ||
| rs748135905 | 0.925 | 0.120 | 1 | 152309045 | stop gained | C/A;T | snv | 4.0E-06; 2.8E-05 | 2 | ||
| rs877776 | 0.925 | 0.120 | 1 | 152205542 | intron variant | C/G;T | snv | 2 | |||
| rs10888499 | 1.000 | 0.120 | 1 | 152560266 | intergenic variant | C/A;T | snv | 1 | |||
| rs11205006 | 1.000 | 0.120 | 1 | 152467700 | intergenic variant | A/T | snv | 0.72 | 1 | ||
| rs12144049 | 1.000 | 0.120 | 1 | 152468434 | intergenic variant | C/G;T | snv | 1 | |||
| rs471144 | 1.000 | 0.120 | 1 | 152481779 | intergenic variant | T/G | snv | 8.0E-02 | 1 | ||
| rs55879323 | 1.000 | 0.120 | 1 | 152196264 | intron variant | C/T | snv | 0.42 | 1 | ||
| rs61813875 | 1.000 | 0.120 | 1 | 152564174 | downstream gene variant | C/G | snv | 1.6E-02 | 1 | ||
| rs6661961 | 1.000 | 0.120 | 1 | 152469813 | intergenic variant | T/A;C | snv | 1 | |||
| rs6686734 | 1.000 | 0.120 | 1 | 12008884 | intron variant | T/C | snv | 0.71 | 1 | ||
| rs77199844 | 1.000 | 0.120 | 1 | 152784619 | upstream gene variant | AT/- | del | 0.12 | 1 | ||
| rs9050 | 1.000 | 0.120 | 1 | 152106838 | 3 prime UTR variant | C/A | snv | 4.3E-02 | 1 | ||
| rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 19 | |
| rs13015714 | 0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 | 3 | ||
| rs574456 | 0.882 | 0.160 | 2 | 140644133 | intron variant | A/T | snv | 8.1E-02 | 3 | ||
| rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 2 |