| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
| rs1800471 | 0.597 | 0.840 | 19 | 41352971 | missense variant | C/G;T | snv | 5.6E-02 | 48 | ||
| rs1617640 | 0.742 | 0.520 | 7 | 100719675 | upstream gene variant | C/A;G;T | snv | 15 | |||
| rs6921438 | 0.776 | 0.360 | 6 | 43957870 | intergenic variant | G/A;C | snv | 10 | |||
| rs1902491 | 0.925 | 0.240 | 4 | 155134181 | intergenic variant | C/A;T | snv | 2 | |||
| rs1065386 | 1.000 | 0.160 | 6 | 31356770 | missense variant | G/A;C;T | snv | 0.34; 5.6E-06 | 1 | ||
| rs11201335 | 1.000 | 0.160 | 10 | 85018443 | intergenic variant | C/G;T | snv | 1 | |||
| rs1144964 | 1.000 | 0.160 | 12 | 68944857 | intron variant | G/C;T | snv | 1 | |||
| rs137949823 | 1.000 | 0.160 | 5 | 43743007 | intergenic variant | G/A;T | snv | 1 | |||
| rs2064196 | 1.000 | 0.160 | 6 | 144266047 | intergenic variant | C/G;T | snv | 1 | |||
| rs3081219 | 1.000 | 0.160 | 15 | 53583969 | intron variant | GAGA/-;GA | delins | 1 | |||
| rs4726066 | 1.000 | 0.160 | 7 | 151625186 | intron variant | G/A;C | snv | 1 | |||
| rs7604016 | 1.000 | 0.160 | 2 | 61965000 | intron variant | T/A;C | snv | 1 | |||
| rs78464534 | 1.000 | 0.160 | 2 | 115234275 | intron variant | C/A;G | snv | 1 | |||
| rs201584991 | 1.000 | 0.160 | 8 | 124979483 | downstream gene variant | ATT/- | delins | 2.6E-04 | 1 | ||
| rs184340784 | 0.925 | 0.160 | 1 | 4529823 | intergenic variant | C/T | snv | 6.1E-04 | 2 | ||
| rs149201869 | 1.000 | 0.160 | 2 | 215487796 | downstream gene variant | T/A | snv | 2.4E-03 | 1 | ||
| rs138683663 | 1.000 | 0.160 | 18 | 59195550 | intergenic variant | C/T | snv | 4.2E-03 | 1 | ||
| rs200295620 | 0.925 | 0.160 | 3 | 168172398 | intergenic variant | T/-;TT | delins | 5.7E-03 | 2 | ||
| rs115523882 | 1.000 | 0.160 | 3 | 168158417 | intergenic variant | A/G | snv | 9.5E-03 | 1 | ||
| rs75348186 | 1.000 | 0.160 | 10 | 36782685 | intergenic variant | T/C | snv | 1.5E-02 | 1 | ||
| rs74161190 | 1.000 | 0.160 | 10 | 130737530 | intergenic variant | A/G | snv | 1.9E-02 | 1 | ||
| rs114921230 | 1.000 | 0.160 | 1 | 226595161 | intron variant | G/A | snv | 3.6E-02 | 1 | ||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs74705672 | 1.000 | 0.160 | 8 | 132042380 | intron variant | A/T | snv | 4.9E-02 | 1 |