| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2523608 | 0.925 | 0.040 | 6 | 31354782 | non coding transcript exon variant | G/A | snv | 0.19 | 6 | ||
| rs920435389 | 1.000 | 0.040 | 5 | 177091064 | missense variant | G/C | snv | 3 | |||
| rs121918392 | 0.925 | 0.040 | 19 | 44907777 | missense variant | G/A | snv | 3.6E-05 | 7.0E-06 | 2 | |
| rs8450 | 1.000 | 0.040 | 1 | 153947810 | 3 prime UTR variant | G/A | snv | 0.27 | 2 | ||
| rs1251035592 | 1.000 | 0.040 | 7 | 99664039 | missense variant | T/C | snv | 4.2E-06 | 1 | ||
| rs1341991169 | 1.000 | 0.040 | 8 | 19939444 | missense variant | G/A | snv | 1 | |||
| rs1444332461 | 1.000 | 0.040 | 22 | 50627185 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs3829462 | 1.000 | 0.040 | 15 | 58560880 | missense variant | C/A;T | snv | 0.97 | 1 | ||
| rs886916693 | 1.000 | 0.040 | 2 | 8806360 | missense variant | T/C | snv | 4.1E-06 | 1 | ||
| rs974389711 | 1.000 | 0.040 | 11 | 116836210 | synonymous variant | C/T | snv | 1 | |||
| rs679899 | 0.925 | 0.080 | 2 | 21028042 | missense variant | G/A | snv | 0.49 | 0.39 | 7 | |
| rs2811712 | 0.882 | 0.080 | 9 | 21998036 | intron variant | G/A | snv | 0.85 | 5 | ||
| rs2222823 | 0.925 | 0.080 | 3 | 123885940 | upstream gene variant | T/A | snv | 0.14 | 4 | ||
| rs17249754 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 12 | ||
| rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 12 | ||
| rs267606661 | 0.763 | 0.120 | 19 | 44909101 | missense variant | C/G;T | snv | 3.9E-04; 1.0E-05 | 10 | ||
| rs769455 | 0.827 | 0.120 | 19 | 44908783 | missense variant | C/T | snv | 1.4E-03 | 6.9E-03 | 8 | |
| rs4973768 | 0.807 | 0.120 | 3 | 27374522 | 3 prime UTR variant | C/T | snv | 0.44 | 7 | ||
| rs4757268 | 0.827 | 0.120 | 11 | 14789216 | synonymous variant | A/G | snv | 0.63 | 0.64 | 6 | |
| rs140808909 | 0.851 | 0.120 | 19 | 44909080 | missense variant | G/A | snv | 2.0E-04 | 5.6E-05 | 5 | |
| rs879254840 | 0.827 | 0.120 | 19 | 11113322 | missense variant | A/G | snv | 5 | |||
| rs1941404 | 0.882 | 0.120 | 11 | 114298316 | non coding transcript exon variant | A/G | snv | 0.59 | 3 | ||
| rs6078 | 0.882 | 0.120 | 15 | 58541794 | missense variant | G/A;T | snv | 7.1E-02; 8.0E-06 | 3 | ||
| rs632793 | 0.882 | 0.120 | 1 | 11850620 | upstream gene variant | A/G | snv | 0.45 | 3 | ||
| rs2071410 | 0.882 | 0.160 | 15 | 90877710 | intron variant | C/A;G;T | snv | 7 |