Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |
rs2281611 | 0.925 | 0.080 | 14 | 101033612 | intron variant | G/A;T | snv | 2 | |||
rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
rs1419316960 | 0.925 | 0.080 | 19 | 10166651 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs823920 | 0.925 | 0.080 | 9 | 101900303 | intergenic variant | A/G | snv | 0.12 | 2 | ||
rs35060588 | 0.925 | 0.080 | 3 | 10213318 | missense variant | C/G;T | snv | 5.5E-02; 1.6E-05 | 2 | ||
rs1215486792 | 0.925 | 0.080 | 14 | 102229572 | missense variant | C/G | snv | 7.0E-06 | 2 | ||
rs11704 | 0.925 | 0.080 | 14 | 102342318 | 3 prime UTR variant | G/C | snv | 0.26 | 2 | ||
rs2946834 | 0.807 | 0.200 | 12 | 102394036 | non coding transcript exon variant | A/G | snv | 0.63 | 7 | ||
rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 26 | ||
rs867538330 | 0.925 | 0.080 | 5 | 102458457 | synonymous variant | C/T | snv | 2 | |||
rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
rs750521832 | 0.732 | 0.200 | 11 | 102718452 | missense variant | A/G | snv | 4.0E-06 | 14 | ||
rs10883782 | 0.925 | 0.080 | 10 | 102824175 | intron variant | A/G | snv | 0.14 | 2 | ||
rs17724534 | 0.925 | 0.080 | 10 | 102845764 | non coding transcript exon variant | C/T | snv | 9.1E-02 | 2 | ||
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 | |
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs2302615 | 0.807 | 0.120 | 2 | 10448012 | intron variant | C/T | snv | 0.31 | 7 |