| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3814399 | 1.000 | 0.080 | 3 | 113272645 | synonymous variant | C/A;T | snv | 4.7E-04; 2.1E-02 | 1 | ||
| rs10175070 | 1.000 | 0.080 | 2 | 227805859 | 5 prime UTR variant | G/A;C | snv | 1 | |||
| rs7793837 | 1.000 | 0.080 | 7 | 30687161 | intron variant | A/C;T | snv | 1 | |||
| rs2292527 | 1.000 | 0.080 | 17 | 17222727 | non coding transcript exon variant | G/A | snv | 3.6E-02 | 1 | ||
| rs7315121 | 1.000 | 0.080 | 12 | 54081158 | intron variant | C/T | snv | 2.8E-02 | 1 | ||
| rs12750027 | 1.000 | 0.080 | 1 | 212883085 | intron variant | G/A | snv | 4.3E-02 | 1 | ||
| rs2313640 | 1.000 | 0.080 | 17 | 39955592 | intron variant | C/T | snv | 0.69 | 1 | ||
| rs7218742 | 1.000 | 0.080 | 17 | 39958108 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs8076474 | 1.000 | 0.080 | 17 | 39954981 | intron variant | G/C | snv | 0.69 | 1 | ||
| rs111789468 | 1.000 | 0.080 | 6 | 33066047 | non coding transcript exon variant | C/T | snv | 0.21 | 1 | ||
| rs3791244 | 1.000 | 0.080 | 2 | 137974195 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs12570188 | 1.000 | 0.080 | 10 | 99095945 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
| rs1220579705 | 1.000 | 0.080 | 5 | 132674079 | missense variant | C/T | snv | 1 | |||
| rs4679858 | 1.000 | 0.080 | 3 | 159428036 | intron variant | A/G | snv | 0.16 | 1 | ||
| rs4473914 | 1.000 | 0.080 | 7 | 20386640 | intron variant | T/C | snv | 0.37 | 1 | ||
| rs917115 | 1.000 | 0.080 | 7 | 28132967 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs59289606 | 1.000 | 0.080 | 9 | 112563085 | intron variant | C/A | snv | 0.16 | 1 | ||
| rs2051809 | 1.000 | 0.080 | 5 | 132721182 | intron variant | A/C | snv | 0.58 | 1 | ||
| rs16925517 | 1.000 | 0.080 | 9 | 106484720 | intron variant | G/A;C | snv | 1 | |||
| rs2037986 | 1.000 | 0.080 | 21 | 28104158 | intron variant | G/T | snv | 0.44 | 1 | ||
| rs912425 | 1.000 | 0.080 | 13 | 42423188 | intron variant | G/A | snv | 0.78 | 1 | ||
| rs4695314 | 1.000 | 0.080 | 4 | 47930644 | intron variant | G/A | snv | 4.6E-02 | 1 | ||
| rs9914220 | 1.000 | 0.080 | 17 | 78366809 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs7770848 | 1.000 | 0.080 | 6 | 44801500 | intron variant | T/G | snv | 3.1E-02 | 1 | ||
| rs4807630 | 1.000 | 0.080 | 19 | 1170446 | intron variant | C/T | snv | 0.26 | 1 |