| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12321966 | 1.000 | 0.080 | 12 | 8548569 | non coding transcript exon variant | G/T | snv | 9.4E-02 | 1 | ||
| rs6560480 | 1.000 | 0.080 | 9 | 75984217 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs7843437 | 1.000 | 0.080 | 8 | 69925162 | upstream gene variant | C/A | snv | 0.30 | 1 | ||
| rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 9 | ||
| rs103294 | 0.827 | 0.200 | 19 | 54293995 | downstream gene variant | T/C | snv | 0.82 | 7 | ||
| rs11666543 | 1.000 | 0.080 | 19 | 54208113 | intron variant | A/G | snv | 0.78 | 1 | ||
| rs12980600 | 1.000 | 0.080 | 19 | 54203380 | intron variant | T/A | snv | 0.79 | 1 | ||
| rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 | |
| rs104895476 | 0.925 | 0.160 | 16 | 50711057 | missense variant | C/G;T | snv | 4.8E-05 | 2 | ||
| rs7603494 | 1.000 | 0.080 | 2 | 47676957 | intergenic variant | C/T | snv | 0.57 | 1 | ||
| rs665268 | 0.882 | 0.160 | 17 | 42570011 | missense variant | A/G | snv | 0.28 | 0.25 | 3 | |
| rs4817988 | 1.000 | 0.080 | 21 | 39096912 | regulatory region variant | G/A | snv | 0.26 | 1 | ||
| rs2836878 | 0.851 | 0.200 | 21 | 39093608 | intergenic variant | G/A | snv | 0.23 | 7 | ||
| rs4817984 | 1.000 | 0.080 | 21 | 39093140 | intergenic variant | C/A;G | snv | 2 | |||
| rs1383258 | 0.925 | 0.160 | 6 | 32815628 | intron variant | C/T | snv | 8.3E-02 | 2 | ||
| rs113452171 | 1.000 | 0.080 | 6 | 32658490 | upstream gene variant | G/T | snv | 1 | |||
| rs9271539 | 1.000 | 0.080 | 6 | 32622251 | regulatory region variant | G/A | snv | 0.36 | 1 | ||
| rs8111 | 0.925 | 0.160 | 6 | 32115398 | 3 prime UTR variant | C/T | snv | 0.26 | 3 | ||
| rs41267090 | 1.000 | 0.080 | 6 | 31880663 | non coding transcript exon variant | A/G;T | snv | 8.0E-06; 4.5E-02 | 1 | ||
| rs28399987 | 1.000 | 0.080 | 6 | 31762974 | 3 prime UTR variant | G/A | snv | 6.5E-03 | 1 | ||
| rs2736173 | 1.000 | 0.080 | 6 | 31621958 | intron variant | C/T | snv | 1.7E-02 | 1 | ||
| rs114202986 | 1.000 | 0.080 | 6 | 31408140 | intron variant | T/A;C | snv | 1 | |||
| rs3763288 | 0.925 | 0.160 | 6 | 31402590 | non coding transcript exon variant | G/A | snv | 5.3E-02 | 2 | ||
| rs12524487 | 0.925 | 0.160 | 6 | 31386461 | upstream gene variant | C/T | snv | 5.9E-02 | 3 | ||
| rs9266745 | 1.000 | 0.080 | 6 | 31383435 | upstream gene variant | G/A | snv | 0.71 | 1 |