Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 23 | ||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 10 | ||
rs11075990 | 0.925 | 0.120 | 16 | 53785981 | intron variant | A/G | snv | 0.41 | 6 | ||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 11 | |||
rs11651052 | 0.851 | 0.200 | 17 | 37742390 | intron variant | G/A | snv | 0.50 | 7 | ||
rs11671664 | 0.925 | 0.120 | 19 | 45669020 | intron variant | G/A | snv | 0.12 | 4 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 6 | ||
rs11709077 | 0.925 | 0.120 | 3 | 12295008 | intron variant | G/A | snv | 8.8E-02 | 3 | ||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 7 | |||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 16 | ||
rs1470579 | 0.925 | 0.160 | 3 | 185811292 | intron variant | A/C | snv | 0.46 | 4 | ||
rs17817964 | 0.925 | 0.120 | 16 | 53794154 | intron variant | C/T | snv | 0.30 | 6 | ||
rs1899951 | 0.851 | 0.160 | 3 | 12353341 | intron variant | C/T | snv | 0.26 | 2 | ||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 4 | ||
rs2237892 | 0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 | 5 | ||
rs2237897 | 0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 | 3 | ||
rs2246012 | 1.000 | 0.080 | 6 | 131577068 | intron variant | T/A;C | snv | 2 | |||
rs2299383 | 1.000 | 0.080 | 7 | 103778399 | intron variant | C/T | snv | 0.41 | 2 | ||
rs329122 | 1.000 | 0.080 | 5 | 134528909 | intron variant | G/A | snv | 0.45 | 2 | ||
rs35261542 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 3 | ||
rs3751812 | 0.882 | 0.160 | 16 | 53784548 | intron variant | G/T | snv | 0.30 | 7 | ||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 19 | |||
rs4865796 | 1.000 | 0.080 | 5 | 53976834 | intron variant | G/A | snv | 0.72 | 3 | ||
rs6947395 | 1.000 | 0.080 | 7 | 69941675 | intron variant | A/T | snv | 0.20 | 2 | ||
rs7034200 | 1.000 | 0.080 | 9 | 4289050 | intron variant | C/A;G | snv | 3 |