Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 10 | ||
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs1980493 | 0.776 | 0.400 | 6 | 32395438 | intron variant | T/C | snv | 0.13 | 6 | ||
rs2855812 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 6 | ||
rs3131296 | 0.807 | 0.320 | 6 | 32205216 | intron variant | C/T | snv | 0.11 | 6 | ||
rs3131379 | 0.752 | 0.440 | 6 | 31753256 | intron variant | G/A | snv | 6.4E-02 | 7.9E-02 | 6 | |
rs558702 | 0.807 | 0.320 | 6 | 31902549 | intron variant | G/A | snv | 7.7E-02 | 6 | ||
rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
rs3130564 | 0.790 | 0.360 | 6 | 31133897 | intron variant | C/T | snv | 0.14 | 5 | ||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 5 | ||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 5 | |||
rs204990 | 0.851 | 0.280 | 6 | 32193653 | intron variant | C/A;T | snv | 4 | |||
rs3129939 | 0.827 | 0.360 | 6 | 32368989 | intron variant | A/G | snv | 0.14 | 4 | ||
rs1265159 | 0.882 | 0.240 | 6 | 31172270 | intron variant | G/A | snv | 0.21 | 2 | ||
rs1422673 | 0.925 | 0.160 | 5 | 151059427 | intron variant | C/G;T | snv | 2 | |||
rs2233287 | 0.925 | 0.160 | 5 | 151060536 | intron variant | G/A | snv | 0.11 | 2 | ||
rs887464 | 0.925 | 0.200 | 6 | 31178143 | intron variant | C/A;T | snv | 2 | |||
rs2071591 | 0.925 | 0.160 | 6 | 31548022 | intron variant | G/A;C | snv | 1 | |||
rs3792783 | 0.882 | 0.280 | 5 | 151076171 | intron variant | A/G | snv | 0.25 | 1 | ||
rs3792785 | 1.000 | 0.120 | 5 | 151072089 | intron variant | T/C | snv | 0.13 | 1 | ||
rs4958881 | 0.827 | 0.280 | 5 | 151070675 | intron variant | T/C | snv | 0.21 | 1 | ||
rs1794282 | 0.807 | 0.320 | 6 | 32698749 | intergenic variant | C/T | snv | 6.4E-02 | 6 | ||
rs2857595 | 0.827 | 0.320 | 6 | 31600692 | intergenic variant | G/A | snv | 0.27 | 6 |