| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7186053 | 1.000 | 0.080 | 16 | 68805390 | intron variant | A/G | snv | 0.69 | 1 | ||
| rs1187825488 | 1.000 | 0.080 | 3 | 75737670 | frameshift variant | TT/- | del | 7.9E-04 | 1 | ||
| rs11889031 | 1.000 | 0.080 | 2 | 203934671 | upstream gene variant | C/T | snv | 0.15 | 1 | ||
| rs34904192 | 1.000 | 0.080 | 21 | 25569623 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs761797378 | 1.000 | 0.080 | 3 | 75737671 | missense variant | T/A | snv | 2.0E-05 | 2.0E-05 | 1 | |
| rs3760469 | 1.000 | 0.080 | 17 | 51153191 | upstream gene variant | T/G | snv | 0.55 | 1 | ||
| rs1190271 | 1.000 | 0.080 | 6 | 105176946 | intron variant | G/A;C | snv | 1 | |||
| rs559635697 | 1.000 | 0.080 | 8 | 23007068 | missense variant | C/A;T | snv | 2.8E-05 | 1 | ||
| rs778962647 | 1.000 | 0.080 | 8 | 91986282 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs11581557 | 1.000 | 0.080 | 1 | 39862786 | intron variant | A/C;T | snv | 1 | |||
| rs9302752 | 0.925 | 0.120 | 16 | 50685192 | upstream gene variant | T/C | snv | 0.68 | 2 | ||
| rs14304 | 1.000 | 0.080 | 17 | 36071135 | 3 prime UTR variant | T/C | snv | 0.78 | 2 | ||
| rs10420252 | 1.000 | 0.080 | 19 | 35648270 | upstream gene variant | G/A | snv | 9.7E-02 | 2 | ||
| rs6510502 | 1.000 | 0.080 | 19 | 35647577 | upstream gene variant | A/C;G | snv | 2 | |||
| rs7166348 | 1.000 | 0.080 | 15 | 98704566 | intron variant | G/A;T | snv | 0.21 | 2 | ||
| rs57698689 | 1.000 | 0.080 | 12 | 25205729 | 3 prime UTR variant | TT/-;T | delins | 0.48 | 2 | ||
| rs11600655 | 0.925 | 0.120 | 11 | 63606853 | intron variant | G/C | snv | 0.27 | 2 | ||
| rs7628626 | 0.925 | 0.120 | 3 | 119525574 | 3 prime UTR variant | A/C | snv | 0.82 | 2 | ||
| rs8105637 | 0.925 | 0.120 | 19 | 5566221 | intron variant | A/G | snv | 0.56 | 2 | ||
| rs2288496 | 0.925 | 0.120 | 14 | 81145770 | 3 prime UTR variant | T/C | snv | 0.39 | 2 | ||
| rs4705341 | 0.882 | 0.120 | 5 | 149426373 | non coding transcript exon variant | A/G | snv | 0.13 | 3 | ||
| rs1455751791 | 0.882 | 0.120 | 6 | 152011735 | synonymous variant | C/G | snv | 4.0E-06 | 3 | ||
| rs1256054 | 0.882 | 0.120 | 14 | 64249595 | synonymous variant | G/C | snv | 2.8E-03 | 9.6E-04 | 3 | |
| rs3801004 | 0.882 | 0.120 | 7 | 5598591 | intron variant | C/A;G;T | snv | 3 | |||
| rs560890523 | 1.000 | 0.080 | 12 | 25205729 | 3 prime UTR variant | TT/-;T | delins | 3 |