| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs987525 | 0.807 | 0.160 | 8 | 128933908 | intron variant | C/A | snv | 0.31 | 7 | ||
| rs9651495 | 1.000 | 0.040 | 10 | 89172624 | regulatory region variant | G/A | snv | 0.13 | 1 | ||
| rs9557210 | 1.000 | 0.040 | 13 | 99395250 | intergenic variant | G/A | snv | 0.16 | 1 | ||
| rs9383064 | 1.000 | 0.040 | 6 | 15535090 | intron variant | G/C | snv | 0.24 | 1 | ||
| rs937283 | 0.716 | 0.200 | 12 | 68808384 | 5 prime UTR variant | A/G | snv | 0.37 | 19 | ||
| rs920778 | 0.633 | 0.480 | 12 | 53966448 | intron variant | G/A | snv | 0.57 | 36 | ||
| rs886039484 | 0.641 | 0.440 | 17 | 7674888 | missense variant | T/C;G | snv | 32 | |||
| rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
| rs879576 | 1.000 | 0.040 | 22 | 17108356 | missense variant | G/A;C | snv | 0.11 | 1 | ||
| rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
| rs876658657 | 0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 | 25 | ||
| rs868438023 | 0.882 | 0.080 | 15 | 40382906 | missense variant | C/T | snv | 4 | |||
| rs865005 | 1.000 | 0.040 | 9 | 33677060 | non coding transcript exon variant | G/A | snv | 4.2E-02 | 1 | ||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
| rs833061 | 0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv | 42 | |||
| rs8305 | 0.882 | 0.120 | 18 | 54294435 | missense variant | G/A | snv | 0.72 | 0.78 | 4 | |
| rs8178085 | 0.851 | 0.080 | 8 | 47898144 | intron variant | T/G | snv | 2.3E-02 | 4 | ||
| rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 12 | ||
| rs8063761 | 1.000 | 0.040 | 16 | 89961218 | intron variant | A/T | snv | 0.33 | 1 | ||
| rs804270 | 0.882 | 0.080 | 8 | 11770112 | 5 prime UTR variant | G/C;T | snv | 3 | |||
| rs7853346 | 0.851 | 0.200 | 9 | 33676096 | non coding transcript exon variant | C/G | snv | 0.28; 1.2E-05 | 0.32 | 6 | |
| rs779759678 | 1.000 | 0.040 | 3 | 36993556 | missense variant | C/G | snv | 4.0E-06 | 3.5E-05 | 1 | |
| rs779417284 | 1.000 | 0.040 | 9 | 95449149 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs774121564 | 1.000 | 0.040 | 2 | 275197 | missense variant | C/G | snv | 4.1E-06 | 1 | ||
| rs773132865 | 1.000 | 0.040 | 16 | 30783312 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 |