| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35603048 | 0.851 | 0.160 | 15 | 40099764 | intron variant | C/A;G;T | snv | 4 | |||
| rs4525246 | 0.851 | 0.160 | 11 | 123524538 | intron variant | G/A;C | snv | 4 | |||
| rs9392017 | 0.851 | 0.160 | 6 | 442357 | intergenic variant | G/A;C | snv | 4 | |||
| rs1860661 | 0.882 | 0.120 | 19 | 1650135 | intron variant | A/C;G | snv | 6.7E-06; 0.54 | 3 | ||
| rs649775 | 0.882 | 0.120 | 6 | 33716536 | upstream gene variant | A/G;T | snv | 3 | |||
| rs181997 | 0.925 | 0.160 | 6 | 32932941 | downstream gene variant | G/A;C | snv | 2 | |||
| rs7745098 | 1.000 | 0.120 | 6 | 135093866 | intron variant | C/G;T | snv | 2 | |||
| rs1244186 | 1.000 | 0.120 | 10 | 8050720 | non coding transcript exon variant | T/A;C | snv | 1 | |||
| rs2240064 | 1.000 | 0.120 | 6 | 31146796 | intron variant | G/A;T | snv | 1 | |||
| rs485411 | 1.000 | 0.120 | 10 | 8051222 | non coding transcript exon variant | T/A;C;G | snv | 0.81 | 1 | ||
| rs6565176 | 1.000 | 0.120 | 16 | 30163605 | intergenic variant | T/A;C | snv | 1 | |||
| rs9267947 | 1.000 | 0.120 | 6 | 32243441 | intergenic variant | A/G;T | snv | 1 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 | |
| rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
| rs56302315 | 0.827 | 0.160 | 4 | 55089802 | missense variant | C/T | snv | 5.3E-04 | 4.1E-04 | 5 | |
| rs182123615 | 0.807 | 0.200 | 9 | 5070058 | splice region variant | T/C | snv | 3.6E-04 | 1.1E-03 | 7 | |
| rs181181503 | 0.851 | 0.160 | 12 | 74276187 | intron variant | T/C | snv | 1.5E-03 | 4 | ||
| rs387906223 | 1.000 | 0.120 | 3 | 49171662 | 5 prime UTR variant | C/T | snv | 4.8E-03 | 1 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs73005220 | 0.851 | 0.160 | 19 | 16161878 | intron variant | A/G | snv | 3.9E-02 | 4 | ||
| rs12621278 | 0.790 | 0.280 | 2 | 172446825 | intron variant | A/G | snv | 4.9E-02 | 7 | ||
| rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 | |
| rs2273773 | 0.790 | 0.360 | 10 | 67906841 | synonymous variant | T/C | snv | 0.11 | 7.1E-02 | 9 |