Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
rs1805054 | 0.708 | 0.200 | 1 | 19666020 | synonymous variant | C/T | snv | 0.15; 8.0E-06 | 0.16 | 17 | |
rs5930 | 0.827 | 0.200 | 19 | 11113589 | synonymous variant | A/G | snv | 0.63 | 0.66 | 8 | |
rs63750577 | 0.827 | 0.120 | 14 | 73186881 | missense variant | C/T | snv | 8 | |||
rs9875793 | 0.925 | 0.080 | 3 | 170968784 | intron variant | A/G | snv | 0.14 | 3 | ||
rs6494223 | 0.882 | 0.120 | 15 | 32104256 | intron variant | C/T | snv | 0.43 | 3 | ||
rs10883866 | 0.882 | 0.160 | 10 | 81883883 | intron variant | C/A;G;T | snv | 3 | |||
rs2153674 | 1.000 | 0.040 | 13 | 105478789 | intron variant | C/T | snv | 0.57 | 1 | ||
rs5905587 | 1.000 | 0.040 | X | 43974750 | upstream gene variant | T/C | snv | 1 |