| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7654093 | 0.882 | 0.120 | 4 | 154623920 | upstream gene variant | A/T | snv | 0.27 | 6 | ||
| rs113092656 | 0.882 | 0.120 | 6 | 11615072 | intergenic variant | G/A | snv | 2.6E-02 | 5 | ||
| rs60942712 | 0.882 | 0.120 | 3 | 88998609 | intergenic variant | G/T | snv | 7.9E-02 | 5 | ||
| rs2089252 | 1.000 | 0.040 | 4 | 75909495 | downstream gene variant | T/C | snv | 2.5E-02 | 1 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 13 | |||
| rs747418061 | 0.807 | 0.200 | 5 | 112828920 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 10 | |
| rs13306190 | 0.807 | 0.320 | 2 | 21032408 | missense variant | G/A;C;T | snv | 1.7E-04; 8.0E-06 | 7 | ||
| rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 40 | ||
| rs72798544 | 0.882 | 0.120 | 2 | 42372465 | intron variant | T/G | snv | 1.3E-02 | 5 | ||
| rs3742264 | 0.742 | 0.400 | 13 | 46073959 | missense variant | C/T | snv | 0.31 | 0.35 | 17 | |
| rs1926447 | 0.807 | 0.440 | 13 | 46055809 | missense variant | A/G | snv | 0.74 | 0.77 | 11 | |
| rs13146272 | 1.000 | 0.040 | 4 | 186199057 | missense variant | C/A | snv | 0.57 | 0.61 | 3 | |
| rs747301897 | 1.000 | 0.040 | 19 | 45363999 | synonymous variant | G/A | snv | 7.1E-06 | 3 | ||
| rs200960801 | 0.827 | 0.200 | 6 | 151944488 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
| rs1248438558 | 0.925 | 0.120 | 13 | 113149020 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs2036914 | 0.882 | 0.160 | 4 | 186271327 | intron variant | T/C | snv | 0.57 | 5 | ||
| rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 7 | |||
| rs2289252 | 1.000 | 0.040 | 4 | 186286227 | non coding transcript exon variant | C/T | snv | 0.35 | 4 | ||
| rs5985 | 0.724 | 0.280 | 6 | 6318562 | missense variant | C/A;T | snv | 0.20; 2.4E-05 | 20 | ||
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
| rs1799963 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 25 | ||
| rs1183194405 | 0.716 | 0.440 | 11 | 46719773 | missense variant | G/A;T | snv | 4.5E-06; 4.5E-06 | 19 | ||
| rs552953108 | 0.724 | 0.200 | 11 | 46729529 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 16 |