Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 6 | ||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 4 | ||
rs2191349 | 1.000 | 0.080 | 7 | 15024684 | intergenic variant | G/T | snv | 0.54 | 4 | ||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
rs1470579 | 0.925 | 0.160 | 3 | 185811292 | intron variant | A/C | snv | 0.46 | 3 | ||
rs7173964 | 1.000 | 0.080 | 15 | 62104743 | regulatory region variant | G/A | snv | 0.49 | 2 |