| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13117307 | 0.827 | 0.080 | 4 | 55885574 | intron variant | C/T | snv | 0.21 | 6 | ||
| rs750553272 | 0.851 | 0.080 | 2 | 177230898 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 4 | |
| rs9277952 | 0.851 | 0.080 | 6 | 33236497 | upstream gene variant | G/A | snv | 0.10 | 4 | ||
| rs2029167 | 0.925 | 0.080 | 12 | 54196349 | intergenic variant | G/A | snv | 0.52 | 3 | ||
| rs10420685 | 1.000 | 0.080 | 19 | 40729215 | synonymous variant | A/G | snv | 7.2E-02 | 9.7E-02 | 1 | |
| rs12494623 | 1.000 | 0.080 | 3 | 179214763 | intron variant | C/G;T | snv | 1 | |||
| rs2029166 | 1.000 | 0.080 | 12 | 54196315 | intergenic variant | C/T | snv | 0.33 | 1 | ||
| rs2229546 | 1.000 | 0.080 | 1 | 67395837 | synonymous variant | C/A;G;T | snv | 0.63; 1.2E-05; 2.4E-05 | 1 | ||
| rs3024656 | 1.000 | 0.080 | 16 | 27358288 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs3181224 | 1.000 | 0.080 | 5 | 159313842 | intron variant | A/G | snv | 0.10 | 1 | ||
| rs3729679 | 1.000 | 0.080 | 3 | 179204642 | intron variant | A/G | snv | 0.58 | 1 | ||
| rs4297265 | 1.000 | 0.080 | 1 | 67386652 | synonymous variant | G/A;T | snv | 1 | |||
| rs7296239 | 1.000 | 0.080 | 12 | 54197920 | intergenic variant | T/C | snv | 0.42 | 1 | ||
| rs853360 | 1.000 | 0.080 | 6 | 14134361 | intron variant | T/C | snv | 0.74 | 1 | ||
| rs246079 | 0.790 | 0.120 | 12 | 109109255 | intron variant | A/G;T | snv | 9 | |||
| rs3219218 | 0.851 | 0.120 | 12 | 109100430 | intron variant | A/G | snv | 1.9E-02 | 4 | ||
| rs4957014 | 0.752 | 0.160 | 5 | 287899 | intron variant | T/G | snv | 0.74 | 11 | ||
| rs3756712 | 0.790 | 0.160 | 5 | 308981 | non coding transcript exon variant | A/C;T | snv | 10 | |||
| rs3087386 | 0.790 | 0.160 | 2 | 99439044 | missense variant | A/G | snv | 0.58 | 0.61 | 8 | |
| rs9298814 | 0.790 | 0.160 | 9 | 21227623 | missense variant | A/C;G | snv | 0.12; 8.8E-06 | 7 | ||
| rs3748079 | 0.925 | 0.160 | 6 | 33620370 | 5 prime UTR variant | C/T | snv | 0.18 | 2 | ||
| rs1049216 | 0.790 | 0.200 | 4 | 184628935 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
| rs28493229 | 0.925 | 0.200 | 19 | 40718299 | intron variant | G/A;C | snv | 6.0E-06; 0.12 | 3 | ||
| rs16997517 | 0.925 | 0.200 | 22 | 36937894 | missense variant | C/T | snv | 2.6E-02 | 4.7E-02 | 2 | |
| rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 12 |