Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1002076 | 0.925 | 0.120 | 1 | 10378834 | 3 prime UTR variant | G/A | snv | 0.33 | 2 | ||
rs7643459 | 0.925 | 0.120 | 3 | 7963141 | intron variant | G/C;T | snv | 2 | |||
rs4525119 | 0.925 | 0.120 | 10 | 5049762 | intron variant | C/T | snv | 0.30 | 2 | ||
rs753461846 | 0.925 | 0.120 | 7 | 1898249 | missense variant | C/A;G;T | snv | 4.0E-06; 2.8E-05 | 2 | ||
rs76032516 | 0.925 | 0.120 | 11 | 96097550 | intron variant | A/C;T | snv | 2 | |||
rs1596797 | 0.925 | 0.120 | 19 | 8977341 | missense variant | T/A;C;G | snv | 2.0E-05; 4.0E-06; 0.74 | 2 | ||
rs146314922 | 0.925 | 0.120 | 19 | 54982828 | missense variant | A/G | snv | 2 | |||
rs11696662 | 0.925 | 0.120 | 20 | 41161795 | intron variant | C/T | snv | 4.4E-02 | 2 | ||
rs2803073 | 0.925 | 0.120 | 6 | 162541796 | intron variant | G/A | snv | 0.74 | 2 | ||
rs17106154 | 0.925 | 0.120 | 14 | 68694457 | non coding transcript exon variant | T/C | snv | 7.8E-02 | 2 | ||
rs1057156 | 0.925 | 0.120 | 3 | 128081228 | 3 prime UTR variant | A/G | snv | 0.22 | 0.23 | 2 | |
rs149652370 | 0.925 | 0.120 | 3 | 128084115 | non coding transcript exon variant | A/G | snv | 1.3E-04 | 2 | ||
rs372150314 | 0.925 | 0.120 | 17 | 18347596 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
rs11175194 | 0.925 | 0.120 | 12 | 63871057 | intron variant | G/A | snv | 0.15 | 2 | ||
rs3087714 | 0.925 | 0.120 | 8 | 69660769 | 3 prime UTR variant | G/A | snv | 0.30 | 2 | ||
rs17329882 | 0.925 | 0.120 | 4 | 119028805 | intron variant | A/C;T | snv | 2 | |||
rs237028 | 0.925 | 0.120 | 6 | 149397514 | intron variant | C/T | snv | 0.58 | 2 | ||
rs17250239 | 0.925 | 0.120 | 9 | 136902178 | non coding transcript exon variant | G/A | snv | 7.2E-02 | 2 | ||
rs10017134 | 0.925 | 0.120 | 4 | 69591303 | intron variant | T/C | snv | 0.75 | 2 | ||
rs7305032 | 0.925 | 0.120 | 12 | 47856077 | intron variant | G/A | snv | 0.61 | 2 | ||
rs4954956 | 0.882 | 0.120 | 2 | 138787007 | regulatory region variant | C/T | snv | 0.25 | 3 | ||
rs7365052 | 0.882 | 0.120 | 1 | 236786561 | intergenic variant | T/C | snv | 3 | |||
rs7748275 | 0.882 | 0.120 | 6 | 3580855 | downstream gene variant | T/A | snv | 8.2E-02 | 3 | ||
rs35068177 | 0.882 | 0.120 | 7 | 87550213 | synonymous variant | T/C | snv | 2.2E-04 | 3.1E-04 | 3 | |
rs186724 | 0.882 | 0.120 | 1 | 110018293 | intron variant | C/G;T | snv | 3 |