Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11554137 | 0.742 | 0.040 | 2 | 208248468 | synonymous variant | G/A | snv | 5.1E-02 | 6.8E-02 | 13 | |
rs1482518887 | 0.790 | 0.040 | 21 | 34887018 | missense variant | C/T | snv | 7.0E-06 | 8 | ||
rs1801020 | 1.000 | 0.040 | 5 | 177409531 | 5 prime UTR variant | A/G | snv | 0.65 | 0.67 | 8 | |
rs138817062 | 0.882 | 0.040 | 15 | 74044940 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 4 | |
rs35602083 | 0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 | 4 | |
rs3842803 | 0.925 | 0.040 | 9 | 122392256 | synonymous variant | T/C | snv | 2.4E-02 | 8.2E-02 | 4 | |
rs652722 | 1.000 | 0.040 | 11 | 31883988 | intron variant | C/T | snv | 0.32 | 4 | ||
rs12133576 | 1.000 | 0.040 | 1 | 93350843 | intron variant | A/G | snv | 0.51 | 3 | ||
rs12199222 | 1.000 | 0.040 | 6 | 17699091 | intron variant | G/A;T | snv | 3 | |||
rs17036328 | 1.000 | 0.040 | 3 | 12348985 | intron variant | T/C | snv | 0.14 | 3 | ||
rs17056278 | 0.925 | 0.040 | 5 | 158825430 | intron variant | C/G | snv | 5.3E-02 | 3 | ||
rs17806888 | 1.000 | 0.040 | 3 | 67365898 | intron variant | T/C | snv | 9.1E-02 | 3 | ||
rs212090 | 1.000 | 0.040 | 16 | 16142147 | 3 prime UTR variant | T/A | snv | 0.36 | 3 | ||
rs2270859 | 1.000 | 0.040 | 3 | 122536861 | non coding transcript exon variant | G/A | snv | 0.14 | 3 | ||
rs233112 | 0.925 | 0.040 | 1 | 85320068 | 3 prime UTR variant | T/C | snv | 0.37 | 3 | ||
rs2597513 | 1.000 | 0.040 | 3 | 13514336 | regulatory region variant | C/T | snv | 0.88 | 3 | ||
rs3213409 | 0.925 | 0.040 | 19 | 17834887 | missense variant | C/T | snv | 8.6E-03 | 7.3E-03 | 3 | |
rs478093 | 1.000 | 0.040 | 1 | 119712503 | 5 prime UTR variant | A/G | snv | 0.73 | 3 | ||
rs4969178 | 1.000 | 0.040 | 17 | 78392121 | intron variant | A/G | snv | 0.63 | 3 | ||
rs4969186 | 1.000 | 0.040 | 17 | 78402323 | intron variant | G/C | snv | 0.62 | 3 | ||
rs602074 | 1.000 | 0.040 | 11 | 31900616 | intron variant | C/T | snv | 0.46 | 3 | ||
rs6088343 | 1.000 | 0.040 | 20 | 33908259 | downstream gene variant | C/T | snv | 0.46 | 3 | ||
rs6142044 | 1.000 | 0.040 | 20 | 33918789 | intergenic variant | A/T | snv | 0.47 | 3 | ||
rs6489785 | 1.000 | 0.040 | 12 | 120925921 | TF binding site variant | T/C | snv | 0.68 | 3 | ||
rs683028 | 1.000 | 0.040 | 11 | 31901029 | intron variant | A/G | snv | 0.44 | 3 |