Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10814916 | 0.851 | 0.200 | 9 | 4293150 | intron variant | A/C | snv | 0.57 | 3 | ||
rs11605924 | 1.000 | 0.080 | 11 | 45851540 | intron variant | A/C | snv | 0.39 | 3 | ||
rs1552224 | 1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 | 3 | ||
rs2292910 | 1.000 | 0.080 | 11 | 45882062 | 3 prime UTR variant | A/C | snv | 0.66 | 2 | ||
rs10278336 | 7 | 44205764 | intron variant | A/C;G | snv | 2 | |||||
rs7867224 | 9 | 4292152 | intron variant | A/C;G | snv | 0.37 | 2 | ||||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs2657879 | 1.000 | 0.080 | 12 | 56471554 | missense variant | A/G | snv | 0.17 | 0.15 | 5 | |
rs2851682 | 11 | 61848540 | intron variant | A/G | snv | 9.9E-02 | 5 | ||||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 4 | ||
rs2305929 | 1.000 | 0.040 | 2 | 27891044 | intron variant | A/G | snv | 0.14 | 3 | ||
rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 3 | ||
rs11619319 | 13 | 27913462 | intron variant | A/G | snv | 0.23 | 2 | ||||
rs118137427 | 10 | 111217250 | intergenic variant | A/G | snv | 3.3E-02 | 2 | ||||
rs2605627 | 11 | 93526349 | intron variant | A/G | snv | 0.79 | 2 | ||||
rs7101470 | 11 | 47032897 | intron variant | A/G | snv | 7.4E-02 | 2 | ||||
rs7713317 | 5 | 96381018 | intron variant | A/G | snv | 0.28 | 2 | ||||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 4 | |||
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 4 | |||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 3 | ||||
rs7944584 | 1.000 | 0.080 | 11 | 47314769 | intron variant | A/T | snv | 0.19 | 3 | ||
rs753993 | 11 | 47328418 | non coding transcript exon variant | C/A | snv | 0.33 | 2 | ||||
rs2302593 | 19 | 45693376 | intron variant | C/A;G | snv | 1.0E-04; 0.48 | 2 | ||||
rs11195502 | 10 | 111279909 | intergenic variant | C/A;G;T | snv | 2 | |||||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 9 |