Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12296850 | 0.925 | 0.080 | 12 | 100426307 | downstream gene variant | A/G | snv | 8.7E-02 | 3 | ||
rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
rs17024869 | 0.708 | 0.320 | 2 | 100843581 | intron variant | T/C | snv | 8.3E-02 | 18 | ||
rs895520 | 0.689 | 0.320 | 2 | 100961475 | intron variant | G/A | snv | 0.35 | 23 | ||
rs7581886 | 0.708 | 0.320 | 2 | 100964784 | intron variant | C/T | snv | 0.92 | 18 | ||
rs4919510 | 0.641 | 0.520 | 10 | 100975021 | mature miRNA variant | C/G | snv | 0.27 | 0.27 | 32 | |
rs6759180 | 1.000 | 0.080 | 2 | 10126436 | intron variant | G/A | snv | 0.74 | 1 | ||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs779901 | 1.000 | 0.080 | 3 | 10228274 | intron variant | C/A;T | snv | 1 | |||
rs12769316 | 0.925 | 0.160 | 10 | 102392994 | upstream gene variant | G/A | snv | 0.13 | 3 | ||
rs5742714 | 0.882 | 0.160 | 12 | 102396074 | 3 prime UTR variant | C/G | snv | 8.9E-02 | 3 | ||
rs7897947 | 1.000 | 0.080 | 10 | 102397954 | intron variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.23 | 1 | ||
rs11574852 | 1.000 | 0.080 | 10 | 102401718 | intron variant | A/C | snv | 2.3E-02 | 2.3E-02 | 1 | |
rs2071230 | 0.882 | 0.080 | 11 | 102790228 | 3 prime UTR variant | A/G | snv | 0.15 | 3 | ||
rs751402 | 0.724 | 0.360 | 13 | 102845848 | 5 prime UTR variant | A/G | snv | 0.76 | 15 | ||
rs2296147 | 0.695 | 0.280 | 13 | 102846025 | 5 prime UTR variant | T/C | snv | 0.38 | 21 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs774188914 | 0.851 | 0.200 | 13 | 102858296 | missense variant | C/G | snv | 2.4E-05 | 1.4E-05 | 4 | |
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs199475643 | 0.882 | 0.240 | 12 | 102894894 | missense variant | T/C | snv | 8.0E-06 | 3 | ||
rs745564626 | 0.752 | 0.280 | 14 | 103699003 | missense variant | C/G;T | snv | 4.3E-05 | 14 | ||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs861537 | 1.000 | 0.080 | 14 | 103700738 | intron variant | C/T | snv | 0.61 | 0.61 | 1 | |
rs1799794 | 0.763 | 0.320 | 14 | 103712930 | splice region variant | T/C | snv | 0.22 | 12 |