Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs367737727 | 1.000 | 0.080 | 14 | 100128600 | missense variant | C/T | snv | 1.1E-05 | 1 | ||
rs773205136 | 1.000 | 0.080 | 2 | 100294302 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
rs7849 | 1.000 | 0.080 | 10 | 100362846 | 3 prime UTR variant | T/C;G | snv | 1 | |||
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 | |
rs367898512 | 1.000 | 0.080 | 10 | 101002900 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 1 | |
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 | ||
rs369664812 | 1.000 | 0.080 | 7 | 101223799 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 1 | |
rs34713741 | 0.882 | 0.280 | 15 | 101277671 | upstream gene variant | C/A;T | snv | 0.24 | 3 | ||
rs1419316960 | 0.925 | 0.080 | 19 | 10166651 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs2186607 | 0.776 | 0.080 | 11 | 101785666 | intron variant | T/A | snv | 0.51 | 10 | ||
rs823920 | 0.925 | 0.080 | 9 | 101900303 | intergenic variant | A/G | snv | 0.12 | 2 | ||
rs990101456 | 1.000 | 0.080 | 10 | 102109138 | missense variant | C/T | snv | 1 | |||
rs537292284 | 1.000 | 0.080 | 10 | 102133102 | missense variant | G/C | snv | 1 | |||
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 | ||
rs1284806277 | 0.827 | 0.200 | 14 | 102251978 | missense variant | A/G | snv | 1.4E-05 | 13 | ||
rs1287689842 | 1.000 | 0.080 | 7 | 102281843 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
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 |