| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762079672 | 0.882 | 0.040 | 1 | 230710211 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
| rs10159239 | 0.882 | 0.040 | 1 | 247443750 | intron variant | G/A | snv | 0.57 | 3 | ||
| rs10918859 | 0.882 | 0.040 | 1 | 162199478 | intron variant | G/A | snv | 0.16 | 3 | ||
| rs12040273 | 0.882 | 0.040 | 1 | 230063651 | intron variant | C/T | snv | 0.28 | 3 | ||
| rs138760780 | 0.882 | 0.040 | 1 | 205515245 | intron variant | C/T | snv | 1.5E-02 | 3 | ||
| rs3045215 | 0.882 | 0.040 | 1 | 234605171 | 3 prime UTR variant | -/GTTACAATA;GTTATAATA | delins | 3 | |||
| rs35511654 | 0.882 | 0.040 | 1 | 111500165 | missense variant | T/G | snv | 9.4E-02 | 9.8E-02 | 3 | |
| rs5705 | 0.882 | 0.040 | 1 | 204162058 | synonymous variant | T/G | snv | 0.14 | 0.18 | 3 | |
| rs6020 | 0.882 | 0.040 | 1 | 169549874 | missense variant | C/T | snv | 0.11 | 0.12 | 3 | |
| rs748954737 | 0.882 | 0.040 | 1 | 159713734 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs756601757 | 0.882 | 0.040 | 1 | 161040847 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
| rs77832441 | 0.882 | 0.040 | 1 | 159714024 | missense variant | G/A | snv | 1.4E-03 | 1.6E-03 | 3 | |
| rs972655070 | 0.882 | 0.040 | 1 | 161040282 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs2292832 | 0.605 | 0.640 | 2 | 240456086 | non coding transcript exon variant | T/A;C | snv | 0.59 | 46 | ||
| rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 30 | ||
| rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 29 | ||
| rs6721961 | 0.672 | 0.520 | 2 | 177265309 | intron variant | T/C;G | snv | 0.89 | 24 | ||
| rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 15 | |||
| rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
| rs4251961 | 0.763 | 0.200 | 2 | 113116890 | intron variant | T/C | snv | 0.29 | 10 | ||
| rs1010 | 0.807 | 0.120 | 2 | 85581859 | 3 prime UTR variant | T/C;G | snv | 7 | |||
| rs1830321 | 0.827 | 0.080 | 2 | 145067988 | intron variant | C/T | snv | 0.40 | 5 | ||
| rs897876 | 0.882 | 0.040 | 2 | 65564447 | intron variant | C/T | snv | 0.30 | 4 | ||
| rs1433748662 | 0.882 | 0.040 | 2 | 8791221 | missense variant | T/C | snv | 3 | |||
| rs371150372 | 0.882 | 0.040 | 2 | 27223972 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 3 |