Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2162679 | 0.851 | 0.240 | 12 | 102477481 | intron variant | C/G;T | snv | 6 | |||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 6 | ||
rs2239186 | 0.882 | 0.120 | 12 | 47875627 | intron variant | A/C;G | snv | 0.17 | 5 | ||
rs2941471 | 0.851 | 0.240 | 8 | 75558169 | intron variant | G/A | snv | 0.65 | 4 | ||
rs3790844 | 0.882 | 0.200 | 1 | 200038304 | intron variant | A/C;G | snv | 4 | |||
rs4759313 | 0.851 | 0.120 | 12 | 53965290 | intron variant | T/A | snv | 0.51 | 4 | ||
rs11644322 | 0.925 | 0.120 | 16 | 79005703 | intron variant | C/T | snv | 0.22 | 3 | ||
rs1537373 | 0.925 | 0.120 | 9 | 22103342 | intron variant | T/G | snv | 0.63 | 3 | ||
rs2001389 | 0.925 | 0.120 | 10 | 102615501 | intron variant | G/A;C | snv | 3 | |||
rs2027605 | 1.000 | 0.120 | 21 | 29354452 | intron variant | A/G | snv | 0.48 | 3 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 3 | ||
rs9363918 | 0.882 | 0.200 | 6 | 68432116 | intron variant | T/G | snv | 0.38 | 3 | ||
rs10500715 | 0.925 | 0.120 | 11 | 9951515 | intron variant | T/G | snv | 0.39 | 2 | ||
rs11085754 | 0.925 | 0.120 | 19 | 11017920 | intron variant | A/G | snv | 0.41 | 2 | ||
rs1153280 | 1.000 | 0.120 | 21 | 29305751 | intron variant | G/A | snv | 0.52 | 2 | ||
rs11644043 | 0.925 | 0.120 | 16 | 50327466 | intron variant | T/C | snv | 0.24 | 2 | ||
rs12362504 | 0.925 | 0.120 | 11 | 9907995 | intron variant | T/C | snv | 0.37 | 2 | ||
rs12456874 | 0.925 | 0.120 | 18 | 13366863 | intron variant | A/G | snv | 0.20 | 2 | ||
rs12939944 | 0.925 | 0.120 | 17 | 12056502 | intron variant | C/T | snv | 0.45 | 2 | ||
rs13303010 | 0.925 | 0.120 | 1 | 959193 | intron variant | G/A | snv | 0.82 | 0.69 | 2 | |
rs1455311 | 0.925 | 0.160 | 4 | 79043433 | intron variant | A/G | snv | 0.14 | 2 | ||
rs1630747 | 0.925 | 0.120 | 21 | 34085692 | intron variant | C/A | snv | 0.69 | 2 | ||
rs17458086 | 0.925 | 0.120 | 12 | 40034837 | intron variant | T/C | snv | 1.1E-02 | 2 | ||
rs1810205 | 0.925 | 0.120 | 10 | 16923228 | intron variant | A/G | snv | 0.47 | 2 | ||
rs2073389 | 0.925 | 0.120 | 22 | 23791306 | intron variant | C/T | snv | 0.59 | 2 |