| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10948155 | 1.000 | 0.040 | 6 | 44720220 | intergenic variant | T/C | snv | 0.30 | 1 | ||
| rs116855380 | 1.000 | 0.040 | 20 | 47491550 | downstream gene variant | A/G | snv | 2.8E-02 | 1 | ||
| rs12154055 | 1.000 | 0.040 | 6 | 44481960 | intergenic variant | G/A | snv | 0.27 | 1 | ||
| rs12618428 | 1.000 | 0.040 | 2 | 150876465 | regulatory region variant | A/G | snv | 0.14 | 1 | ||
| rs12923310 | 1.000 | 0.040 | 16 | 9694080 | intergenic variant | G/T | snv | 0.32 | 1 | ||
| rs150365637 | 1.000 | 0.040 | 8 | 9222261 | intron variant | -/T | delins | 0.13 | 1 | ||
| rs1627411 | 1.000 | 0.040 | 14 | 42702125 | intron variant | T/C | snv | 0.75 | 1 | ||
| rs330050 | 1.000 | 0.040 | 8 | 9230169 | intron variant | G/C;T | snv | 1 | |||
| rs35206230 | 1.000 | 0.040 | 15 | 74805439 | downstream gene variant | C/T | snv | 0.43 | 1 | ||
| rs4140564 | 1.000 | 0.040 | 1 | 186755871 | intergenic variant | G/A | snv | 0.93 | 1 | ||
| rs4764133 | 1.000 | 0.040 | 12 | 14911429 | downstream gene variant | C/G;T | snv | 1 | |||
| rs4931462 | 1.000 | 0.040 | 12 | 31225008 | TF binding site variant | T/G | snv | 0.65 | 1 | ||
| rs6094710 | 1.000 | 0.040 | 20 | 47466905 | intergenic variant | G/A | snv | 5.0E-02 | 1 | ||
| rs614332 | 1.000 | 0.040 | 11 | 93101032 | intergenic variant | C/T | snv | 0.62 | 1 | ||
| rs6766414 | 1.000 | 0.040 | 3 | 31446730 | intergenic variant | T/G | snv | 0.22 | 1 | ||
| rs80057746 | 1.000 | 0.040 | 4 | 78701519 | intergenic variant | C/T | snv | 1.7E-02 | 1 | ||
| rs11807350 | 1.000 | 0.040 | 1 | 161191145 | missense variant | C/T | snv | 3.1E-04 | 4.7E-04 | 1 | |
| rs12915901 | 1.000 | 0.040 | 15 | 57987234 | intron variant | G/A | snv | 0.37 | 1 | ||
| rs3204689 | 1.000 | 0.040 | 15 | 57954604 | 3 prime UTR variant | G/C | snv | 0.37 | 1 | ||
| rs7805536 | 1.000 | 0.040 | 7 | 32533958 | non coding transcript exon variant | T/C | snv | 0.15 | 1 | ||
| rs2353525 | 1.000 | 0.040 | 1 | 147597199 | intron variant | T/G | snv | 0.34 | 1 | ||
| rs3757837 | 1.000 | 0.040 | 7 | 44237052 | intron variant | T/C | snv | 0.15 | 1 | ||
| rs3815148 | 1.000 | 0.040 | 7 | 107297975 | intron variant | A/C | snv | 0.20 | 1 | ||
| rs1034762 | 1.000 | 0.040 | 12 | 47995860 | intron variant | A/C | snv | 0.74 | 0.79 | 1 | |
| rs2070739 | 1.000 | 0.040 | 12 | 47974193 | missense variant | C/T | snv | 0.16 | 1.0E-01 | 1 |