Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7538876 | 0.807 | 0.120 | 1 | 17395867 | intron variant | G/A | snv | 0.37 | 6 | ||
rs801114 | 0.827 | 0.120 | 1 | 228862088 | downstream gene variant | T/G | snv | 0.48 | 5 | ||
rs891835 | 0.851 | 0.120 | 8 | 129479506 | intron variant | T/G | snv | 0.17 | 5 | ||
rs866460345 | 0.882 | 0.120 | 7 | 55143362 | missense variant | C/T | snv | 4 | |||
rs2269432 | 0.882 | 0.120 | 3 | 50296800 | missense variant | T/A;G | snv | 0.13 | 3 | ||
rs258322 | 0.925 | 0.120 | 16 | 89689495 | intron variant | A/G;T | snv | 3 | |||
rs4785763 | 0.925 | 0.120 | 16 | 90000528 | non coding transcript exon variant | A/C;T | snv | 3 | |||
rs1572072 | 1.000 | 0.120 | 13 | 23553071 | intergenic variant | G/T | snv | 0.36 | 2 | ||
rs189897 | 1.000 | 0.120 | 3 | 37477054 | intron variant | T/A | snv | 0.13 | 2 | ||
rs200046052 | 1.000 | 0.120 | 3 | 49902693 | missense variant | C/G;T | snv | 1.8E-04; 3.6E-05 | 2 | ||
rs2305806 | 1.000 | 0.120 | 19 | 6754996 | synonymous variant | T/C | snv | 0.30 | 0.35 | 2 | |
rs2517713 | 1.000 | 0.120 | 6 | 29950322 | downstream gene variant | G/A;T | snv | 2 | |||
rs28421666 | 1.000 | 0.120 | 6 | 32624960 | upstream gene variant | A/G | snv | 6.9E-02 | 2 | ||
rs2860580 | 1.000 | 0.120 | 6 | 29938914 | upstream gene variant | A/C;G;T | snv | 2 | |||
rs3129055 | 1.000 | 0.120 | 6 | 29702484 | regulatory region variant | A/G | snv | 0.24 | 2 | ||
rs417162 | 1.000 | 0.120 | 6 | 29948728 | downstream gene variant | C/T | snv | 0.66 | 2 | ||
rs770251749 | 1.000 | 0.120 | 6 | 54121506 | missense variant | A/C | snv | 4.0E-06 | 2 | ||
rs9510787 | 1.000 | 0.120 | 13 | 23631056 | intron variant | A/G | snv | 0.20 | 2 | ||
rs10163267 | 1.000 | 0.120 | 16 | 83940313 | intron variant | G/A;C | snv | 1 | |||
rs10496040 | 1.000 | 0.120 | 2 | 55080510 | 5 prime UTR variant | C/A | snv | 9.1E-02 | 1 | ||
rs1059449 | 1.000 | 0.120 | 6 | 29942921 | missense variant | G/A | snv | 6.1E-02 | 9.0E-02 | 1 | |
rs11158728 | 1.000 | 0.120 | 14 | 68295488 | intron variant | G/A;C;T | snv | 1 | |||
rs11237828 | 1.000 | 0.120 | 11 | 79422176 | mature miRNA variant | T/C | snv | 0.12 | 0.22 | 1 | |
rs115214213 | 1.000 | 0.120 | 11 | 35231896 | 3 prime UTR variant | T/C | snv | 4.9E-03 | 1 | ||
rs117465650 | 1.000 | 0.120 | 2 | 55050090 | missense variant | C/T | snv | 0.12 | 6.1E-02 | 1 |