Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11564475 | 0.882 | 0.080 | 3 | 41238542 | intron variant | A/G | snv | 3.7E-02 | 3 | ||
rs2293035 | 0.882 | 0.080 | 19 | 43546923 | synonymous variant | G/A | snv | 1.6E-04 | 1.5E-04 | 3 | |
rs4646421 | 0.882 | 0.080 | 15 | 74723851 | intron variant | G/A;C;T | snv | 0.21 | 3 | ||
rs10116253 | 0.851 | 0.120 | 9 | 117702042 | upstream gene variant | T/C | snv | 0.28 | 4 | ||
rs1200055659 | 0.851 | 0.080 | 1 | 153614902 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1057317 | 0.827 | 0.160 | 9 | 117715764 | 3 prime UTR variant | C/A | snv | 5 | |||
rs1870134 | 0.827 | 0.120 | 3 | 14178523 | missense variant | G/C;T | snv | 4.2E-02; 8.1E-06 | 5 | ||
rs621559 | 0.827 | 0.080 | 1 | 43179740 | intron variant | G/A | snv | 0.18 | 5 | ||
rs12108497 | 0.851 | 0.080 | 4 | 184650403 | intron variant | C/G;T | snv | 6 | |||
rs12304647 | 0.807 | 0.160 | 12 | 53991163 | intron variant | A/C | snv | 0.26 | 6 | ||
rs1760893 | 0.807 | 0.080 | 14 | 20412501 | intron variant | C/A | snv | 0.89 | 6 | ||
rs148611340 | 0.790 | 0.120 | 19 | 43543621 | missense variant | G/A;C | snv | 4.0E-06; 1.2E-05 | 7 | ||
rs2303428 | 0.776 | 0.240 | 2 | 47476361 | splice region variant | T/A;C;G | snv | 4.0E-06; 0.12 | 9 | ||
rs2494752 | 0.790 | 0.120 | 14 | 104797271 | upstream gene variant | A/G | snv | 0.85 | 10 | ||
rs398652 | 0.752 | 0.240 | 14 | 56058851 | intergenic variant | G/A | snv | 0.24 | 10 | ||
rs1143633 | 0.752 | 0.280 | 2 | 112832890 | intron variant | C/G;T | snv | 11 | |||
rs6682925 | 0.776 | 0.160 | 1 | 67165579 | intron variant | C/T | snv | 0.47 | 11 | ||
rs5744174 | 0.742 | 0.360 | 1 | 223111186 | missense variant | A/G | snv | 0.39 | 0.34 | 13 | |
rs4135385 | 0.742 | 0.320 | 3 | 41237949 | non coding transcript exon variant | A/G | snv | 0.19 | 14 | ||
rs184003 | 0.724 | 0.400 | 6 | 32182519 | intron variant | C/A | snv | 0.12 | 0.12 | 15 | |
rs751402 | 0.724 | 0.360 | 13 | 102845848 | 5 prime UTR variant | A/G | snv | 0.76 | 15 | ||
rs4072111 | 0.716 | 0.400 | 15 | 81285798 | missense variant | C/T | snv | 0.17 | 0.11 | 16 | |
rs4711998 | 0.708 | 0.360 | 6 | 52185555 | upstream gene variant | A/G | snv | 0.64 | 16 | ||
rs3765524 | 0.724 | 0.320 | 10 | 94298541 | missense variant | C/T | snv | 0.27 | 0.31 | 17 | |
rs3807987 | 0.732 | 0.280 | 7 | 116539780 | intron variant | G/A | snv | 7.6E-02 | 17 |