| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111577701 | 1.000 | 0.040 | 3 | 168143620 | intergenic variant | C/T | snv | 0.13 | 1 | ||
| rs111908689 | 1.000 | 0.040 | 11 | 85938055 | downstream gene variant | C/G;T | snv | 1 | |||
| rs12204701 | 1.000 | 0.040 | 6 | 4644367 | regulatory region variant | G/A | snv | 0.11 | 1 | ||
| rs2717068 | 1.000 | 0.040 | 2 | 57867738 | intergenic variant | A/C | snv | 0.70 | 1 | ||
| rs28498976 | 1.000 | 0.040 | 4 | 31149735 | downstream gene variant | G/A | snv | 0.44 | 1 | ||
| rs2910464 | 1.000 | 0.040 | 5 | 62162171 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs4638568 | 1.000 | 0.040 | 16 | 50011928 | regulatory region variant | G/A | snv | 4.5E-02 | 1 | ||
| rs4895178 | 1.000 | 0.040 | 5 | 121518937 | intergenic variant | G/A | snv | 0.41 | 1 | ||
| rs492146 | 1.000 | 0.040 | 6 | 52971097 | upstream gene variant | G/A | snv | 0.47 | 1 | ||
| rs535066 | 1.000 | 0.040 | 4 | 46238270 | intergenic variant | G/T | snv | 0.62 | 1 | ||
| rs61670327 | 1.000 | 0.040 | 5 | 3276582 | regulatory region variant | G/A | snv | 0.55 | 1 | ||
| rs71547482 | 1.000 | 0.040 | 6 | 103600058 | intergenic variant | -/TGCAATCT | delins | 0.11 | 1 | ||
| rs10234411 | 1.000 | 0.040 | 7 | 87535576 | intron variant | T/A;C;G | snv | 1 | |||
| rs6949448 | 1.000 | 0.040 | 7 | 87512498 | intron variant | T/C | snv | 0.63 | 1 | ||
| rs11214136 | 1.000 | 0.040 | 11 | 112211286 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs9314349 | 1.000 | 0.040 | 8 | 27616685 | upstream gene variant | A/G | snv | 0.30 | 1 | ||
| rs886039278 | 1.000 | 0.040 | 22 | 31815000 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs2229944 | 1.000 | 0.040 | 5 | 161294312 | synonymous variant | G/A | snv | 0.11 | 0.11 | 1 | |
| rs761305470 | 1.000 | 0.040 | 5 | 161294108 | synonymous variant | G/A;T | snv | 2.4E-05; 8.0E-06 | 1 | ||
| rs42938 | 1.000 | 0.040 | 22 | 30569770 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs4840200 | 1.000 | 0.040 | 6 | 101879428 | intron variant | T/C | snv | 7.8E-02 | 1 | ||
| rs9390754 | 1.000 | 0.040 | 6 | 101517038 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs755041031 | 1.000 | 0.040 | 3 | 121799285 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs10030601 | 1.000 | 0.040 | 4 | 149804060 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs61822012 | 1.000 | 0.040 | 1 | 160071368 | intron variant | A/G | snv | 0.22 | 1 |