| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1000731 | 1.000 | 0.040 | 1 | 231827745 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs10014145 | 1.000 | 0.040 | 4 | 102279420 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs10014424 | 1.000 | 0.040 | 4 | 99943207 | intron variant | G/A | snv | 6.2E-02 | 1 | ||
| rs10036665 | 1.000 | 0.040 | 5 | 138252460 | 3 prime UTR variant | T/A | snv | 0.16 | 1 | ||
| rs10042486 | 0.882 | 0.040 | 5 | 63965502 | intron variant | C/T | snv | 0.58 | 4 | ||
| rs10043986 | 0.925 | 0.040 | 5 | 79799594 | missense variant | C/T | snv | 8.7E-02 | 8.2E-02 | 2 | |
| rs10046055 | 1.000 | 0.040 | 5 | 157890009 | regulatory region variant | T/A | snv | 0.32 | 1 | ||
| rs10063995 | 1.000 | 0.040 | 5 | 175445201 | upstream gene variant | G/C;T | snv | 1 | |||
| rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 25 | ||
| rs10074991 | 0.851 | 0.120 | 5 | 40790449 | intron variant | G/A | snv | 0.31 | 5 | ||
| rs10078551 | 1.000 | 0.040 | 5 | 148621907 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs10082463 | 1.000 | 0.040 | 10 | 117261896 | intron variant | A/C;G | snv | 1 | |||
| rs1009153 | 1.000 | 0.040 | 15 | 22896157 | intron variant | C/G;T | snv | 1 | |||
| rs1009382 | 1.000 | 0.040 | 6 | 32058330 | missense variant | C/A;G;T | snv | 0.72 | 1 | ||
| rs10098073 | 1.000 | 0.040 | 8 | 142228143 | intron variant | C/A | snv | 0.35 | 1 | ||
| rs10108011 | 1.000 | 0.040 | 8 | 22463293 | intron variant | G/A | snv | 0.63 | 1 | ||
| rs1011313 | 1.000 | 0.040 | 6 | 15633201 | intron variant | T/A;C | snv | 1 | |||
| rs10137071 | 0.925 | 0.040 | 14 | 54903622 | upstream gene variant | C/G;T | snv | 2 | |||
| rs10141940 | 1.000 | 0.040 | 14 | 33800515 | synonymous variant | C/A;G;T | snv | 0.13 | 1 | ||
| rs10142034 | 1.000 | 0.040 | 14 | 33800569 | synonymous variant | C/G | snv | 0.12 | 0.12 | 1 | |
| rs1016388 | 1.000 | 0.040 | 12 | 2212702 | intron variant | A/T | snv | 0.53 | 1 | ||
| rs10174400 | 1.000 | 0.040 | 2 | 165268709 | non coding transcript exon variant | C/T | snv | 0.38 | 1 | ||
| rs1018381 | 0.882 | 0.040 | 6 | 15656839 | intron variant | G/A | snv | 0.16 | 6 | ||
| rs10190125 | 1.000 | 0.040 | 2 | 2290654 | intron variant | G/A | snv | 0.34 | 1 | ||
| rs1024582 | 1.000 | 0.040 | 12 | 2293080 | intron variant | A/G;T | snv | 1 |