| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs778036161 | 0.776 | 0.080 | 8 | 92017363 | missense variant | T/C | snv | 8.0E-06 | 9 | ||
| rs560890523 | 1.000 | 0.080 | 12 | 25205729 | 3 prime UTR variant | TT/-;T | delins | 3 | |||
| rs10420252 | 1.000 | 0.080 | 19 | 35648270 | upstream gene variant | G/A | snv | 9.7E-02 | 2 | ||
| rs14304 | 1.000 | 0.080 | 17 | 36071135 | 3 prime UTR variant | T/C | snv | 0.78 | 2 | ||
| rs57698689 | 1.000 | 0.080 | 12 | 25205729 | 3 prime UTR variant | TT/-;T | delins | 0.48 | 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 | ||
| rs11581557 | 1.000 | 0.080 | 1 | 39862786 | intron variant | A/C;T | snv | 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 | ||
| rs1190271 | 1.000 | 0.080 | 6 | 105176946 | intron variant | G/A;C | snv | 1 | |||
| rs34904192 | 1.000 | 0.080 | 21 | 25569623 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs3760469 | 1.000 | 0.080 | 17 | 51153191 | upstream gene variant | T/G | snv | 0.55 | 1 | ||
| rs559635697 | 1.000 | 0.080 | 8 | 23007068 | missense variant | C/A;T | snv | 2.8E-05 | 1 | ||
| rs7186053 | 1.000 | 0.080 | 16 | 68805390 | intron variant | A/G | snv | 0.69 | 1 | ||
| rs761797378 | 1.000 | 0.080 | 3 | 75737671 | missense variant | T/A | snv | 2.0E-05 | 2.0E-05 | 1 | |
| rs778962647 | 1.000 | 0.080 | 8 | 91986282 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs116909374 | 0.776 | 0.120 | 14 | 36269155 | regulatory region variant | C/T | snv | 2.3E-02 | 11 | ||
| rs11064 | 0.807 | 0.120 | 5 | 119393693 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
| rs746429 | 0.882 | 0.120 | 11 | 65649963 | synonymous variant | G/A | snv | 0.31 | 0.30 | 8 | |
| rs12918952 | 0.851 | 0.120 | 16 | 78386878 | missense variant | G/A;C;T | snv | 7 | |||
| rs34214448 | 0.851 | 0.120 | 17 | 51154651 | intron variant | G/T | snv | 0.39 | 7 | ||
| rs11539752 | 0.882 | 0.120 | 14 | 24632383 | missense variant | G/C | snv | 0.21 | 0.26 | 6 | |
| rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 6 | ||
| rs2236142 | 0.827 | 0.120 | 22 | 28741956 | 5 prime UTR variant | G/C | snv | 0.66 | 6 |