Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs874945 | 0.732 | 0.240 | 12 | 53961667 | upstream gene variant | C/T | snv | 0.38 | 14 | ||
rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 9 | ||
rs3814113 | 0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 | 5 | ||
rs633862 | 0.925 | 0.120 | 9 | 133279871 | upstream gene variant | T/C | snv | 0.49 | 5 | ||
rs67397200 | 0.827 | 0.160 | 19 | 17290595 | upstream gene variant | C/G | snv | 0.27 | 5 | ||
rs6785617 | 0.882 | 0.120 | 3 | 172501054 | downstream gene variant | A/T | snv | 3.7E-02 | 4 | ||
rs7313833 | 0.851 | 0.120 | 12 | 27930263 | intergenic variant | G/A | snv | 0.37 | 4 | ||
rs4954956 | 0.882 | 0.120 | 2 | 138787007 | regulatory region variant | C/T | snv | 0.25 | 3 | ||
rs7365052 | 0.882 | 0.120 | 1 | 236786561 | intergenic variant | T/C | snv | 3 | |||
rs7748275 | 0.882 | 0.120 | 6 | 3580855 | downstream gene variant | T/A | snv | 8.2E-02 | 3 | ||
rs1017134 | 0.925 | 0.120 | 7 | 35307237 | intergenic variant | G/A | snv | 0.47 | 2 | ||
rs1192691 | 0.925 | 0.120 | 10 | 36880367 | regulatory region variant | G/T | snv | 0.90 | 2 | ||
rs142091544 | 0.925 | 0.120 | 5 | 168286995 | upstream gene variant | C/T | snv | 2.1E-02 | 2 | ||
rs4286604 | 0.925 | 0.120 | 4 | 69576447 | intron variant | A/G | snv | 0.76 | 2 | ||
rs7501462 | 0.925 | 0.120 | 17 | 16974091 | upstream gene variant | A/G | snv | 0.31 | 2 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs2229109 | 0.807 | 0.240 | 7 | 87550493 | missense variant | C/A;T | snv | 2.7E-02 | 8 | ||
rs533117495 | 0.827 | 0.200 | 7 | 87595783 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
rs35068177 | 0.882 | 0.120 | 7 | 87550213 | synonymous variant | T/C | snv | 2.2E-04 | 3.1E-04 | 3 | |
rs1127313 | 1.000 | 0.120 | 1 | 154583949 | 3 prime UTR variant | G/A | snv | 0.41 | 1 | ||
rs186724 | 0.882 | 0.120 | 1 | 110018293 | intron variant | C/G;T | snv | 3 | |||
rs1955513 | 0.925 | 0.120 | 14 | 32706736 | intron variant | T/G | snv | 0.11 | 2 |