| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10006235 | 1.000 | 0.040 | 4 | 129748953 | non coding transcript exon variant | T/C | snv | 0.73 | 2 | ||
| rs1000731 | 1.000 | 0.040 | 1 | 231827745 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs10012947 | 1.000 | 0.040 | 4 | 30491805 | regulatory region variant | C/T | snv | 0.33 | 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 | ||
| rs1001684 | 1.000 | 0.040 | 5 | 40810324 | intergenic variant | C/A | snv | 0.29 | 1 | ||
| rs1002424 | 1.000 | 0.040 | 5 | 40767295 | intron variant | A/G | snv | 0.31 | 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 | ||
| rs10046758 | 1.000 | 0.040 | 8 | 4326648 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs10061788 | 1.000 | 0.040 | 5 | 88638889 | intron variant | G/A;T | snv | 2 | |||
| rs10063995 | 1.000 | 0.040 | 5 | 175445201 | upstream gene variant | G/C;T | snv | 1 | |||
| rs10065570 | 1.000 | 0.040 | 5 | 40835525 | upstream gene variant | C/T | snv | 0.33 | 1 | ||
| rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 27 | ||
| rs10074991 | 0.851 | 0.120 | 5 | 40790449 | intron variant | G/A | snv | 0.31 | 7 | ||
| rs10077591 | 1.000 | 0.040 | 5 | 165935005 | intergenic variant | C/T | snv | 0.44 | 1 | ||
| rs10078551 | 1.000 | 0.040 | 5 | 148621907 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs1008078 | 1.000 | 0.040 | 1 | 90724174 | non coding transcript exon variant | C/T | snv | 0.33 | 2 | ||
| rs10082463 | 1.000 | 0.040 | 10 | 117261896 | intron variant | A/C;G | snv | 1 | |||
| rs10083370 | 1.000 | 0.040 | 14 | 103847845 | intron variant | G/A | snv | 0.55 | 1 | ||
| rs10085567 | 1.000 | 0.040 | 7 | 76104888 | intron variant | A/C | snv | 0.43 | 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 |