Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10853728 | 0.851 | 0.160 | 19 | 39254506 | downstream gene variant | C/A;G;T | snv | 5 | |||
rs4803217 | 0.882 | 0.120 | 19 | 39243580 | 3 prime UTR variant | C/A | snv | 0.39 | 4 | ||
rs1879026 | 1.000 | 0.080 | 4 | 186079167 | intron variant | G/C;T | snv | 3 | |||
rs2237061 | 1.000 | 0.080 | 5 | 135576640 | intron variant | C/T | snv | 8.4E-02 | 2 | ||
rs17879702 | 1.000 | 0.080 | 6 | 32584346 | missense variant | G/A | snv | 3.2E-02 | 5.7E-02 | 2 | |
rs17568725 | 5 | 171743637 | TF binding site variant | C/A | snv | 0.19 | 1 | ||||
rs9522267 | 13 | 111544020 | intergenic variant | G/A | snv | 0.32 | 1 | ||||
rs10484389 | 6 | 22075033 | intron variant | C/T | snv | 6.0E-02 | 1 | ||||
rs1432133 | 15 | 26983199 | intron variant | A/G;T | snv | 1 | |||||
rs4683336 | 3 | 42818461 | intron variant | C/T | snv | 0.61 | 1 | ||||
rs7518687 | 1 | 168663745 | intergenic variant | A/T | snv | 0.22 | 1 | ||||
rs2174866 | 15 | 53172023 | intergenic variant | A/T | snv | 6.2E-02 | 1 | ||||
rs4467099 | 16 | 11449038 | missense variant | C/A;T | snv | 0.66 | 1 | ||||
rs11025185 | 11 | 19572259 | intron variant | G/A | snv | 2.4E-03 | 1 | ||||
rs8014067 | 14 | 62086539 | intron variant | A/T | snv | 0.79 | 1 | ||||
rs1047782 | 6 | 24650503 | 3 prime UTR variant | T/C;G | snv | 1 | |||||
rs3087943 | 6 | 24650533 | 3 prime UTR variant | A/G | snv | 0.18 | 1 |