Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16896398 | 6 | 43294966 | upstream gene variant | A/T | snv | 0.42 | 5 | ||||
rs11030119 | 11 | 27706555 | intron variant | G/A;T | snv | 3 | |||||
rs11072518 | 15 | 74942269 | upstream gene variant | T/A;C | snv | 3 | |||||
rs2132572 | 1.000 | 7 | 45921946 | upstream gene variant | T/C | snv | 0.79 | 3 | |||
rs7087728 | 10 | 80273714 | 3 prime UTR variant | G/A;C | snv | 3 | |||||
rs864321650 | 5 | 173234902 | missense variant | G/A;C | snv | 3 | |||||
rs1003346 | 1.000 | 9 | 109053060 | intron variant | C/A | snv | 0.43 | 2 | |||
rs1035543 | 16 | 71949873 | missense variant | G/C | snv | 0.39 | 0.33 | 2 | |||
rs12037987 | 1 | 112500200 | intron variant | T/C | snv | 8.6E-02 | 2 | ||||
rs1555729486 | 1.000 | 19 | 15192118 | missense variant | C/A;T | snv | 2 | ||||
rs2073824 | 9 | 133257246 | intron variant | A/G | snv | 0.40 | 2 | ||||
rs2074633 | 7 | 18996297 | 3 prime UTR variant | T/A;C | snv | 2 | |||||
rs218966 | 7 | 10982603 | missense variant | A/G | snv | 0.64 | 0.68 | 2 | |||
rs2285489 | 9 | 133424254 | intron variant | T/C | snv | 0.68 | 2 | ||||
rs3851059 | 10 | 80270902 | downstream gene variant | G/A | snv | 0.27 | 2 | ||||
rs3918166 | 7 | 150996468 | missense variant | G/A;C | snv | 3.9E-03; 8.8E-05 | 2 | ||||
rs556621 | 1.000 | 6 | 44626422 | intergenic variant | T/G | snv | 0.73 | 2 | |||
rs61742245 | 16 | 31094624 | missense variant | C/A;T | snv | 2.4E-03 | 2 | ||||
rs759985000 | 11 | 27700987 | 5 prime UTR variant | G/A;C | snv | 4.2E-06; 8.4E-06 | 2 | ||||
rs773539041 | 1.000 | 19 | 15192289 | missense variant | C/A;T | snv | 2 | ||||
rs8176668 | 9 | 133268647 | intron variant | A/T | snv | 2 | |||||
rs10089084 | 8 | 39912430 | intron variant | G/C | snv | 0.30 | 1 | ||||
rs10123021 | 9 | 100689786 | regulatory region variant | G/A;T | snv | 1 | |||||
rs10414398 | 19 | 44517149 | missense variant | G/A | snv | 0.14 | 0.15 | 1 | |||
rs10478723 | 6 | 12295228 | intron variant | G/A | snv | 0.15 | 1 |