Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs745386663 | 0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 4 | |
rs6780220 | 0.882 | 0.120 | 3 | 33045708 | non coding transcript exon variant | A/C | snv | 0.19 | 3 | ||
rs72555392 | 0.807 | 0.200 | 3 | 33072613 | missense variant | C/T | snv | 3.6E-05 | 3 | ||
rs72555391 | 0.882 | 0.160 | 3 | 33016743 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 3 | |
rs192732174 | 0.827 | 0.160 | 3 | 33068245 | missense variant | G/A;T | snv | 4.0E-05; 3.6E-05 | 2 | ||
rs72555363 | 0.925 | 0.160 | 3 | 33014263 | missense variant | C/A | snv | 2 | |||
rs72555390 | 0.807 | 0.160 | 3 | 33072637 | missense variant | A/G;T | snv | 2 | |||
rs72555362 | 0.925 | 0.160 | 3 | 33051979 | missense variant | C/A | snv | 5.6E-05 | 7.0E-06 | 2 | |
rs761887139 | 0.925 | 0.160 | 3 | 33051997 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
rs34421970 | 0.925 | 0.120 | 3 | 33018489 | missense variant | G/A | snv | 1.1E-02 | 9.4E-03 | 2 | |
rs28934886 | 0.882 | 0.160 | 3 | 33016818 | missense variant | C/T | snv | 1.2E-05 | 2 | ||
rs189115557 | 0.882 | 0.160 | 3 | 33058220 | missense variant | C/T | snv | 6.4E-05 | 4.9E-05 | 1 | |
rs376663785 | 0.827 | 0.160 | 3 | 33051989 | missense variant | A/C | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs73826339 | 1.000 | 0.120 | 3 | 33014196 | missense variant | T/A;C | snv | 4.7E-02 | 1 | ||
rs781658798 | 0.925 | 0.120 | 3 | 33046194 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
rs755581184 | 1.000 | 0.120 | 3 | 32997206 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs72555368 | 0.827 | 0.160 | 3 | 33014292 | missense variant | T/C | snv | 1.2E-05 | 1 | ||
rs201807974 | 1.000 | 0.120 | 3 | 32997296 | missense variant | G/A | snv | 1.2E-04 | 1.1E-04 | 1 | |
rs1553612220 | 1.000 | 0.120 | 3 | 33068968 | missense variant | T/C | snv | 1 | |||
rs775958270 | 1.000 | 0.120 | 3 | 33051980 | missense variant | A/G | snv | 5.6E-05 | 7.0E-06 | 1 | |
rs1356418704 | 1.000 | 0.160 | 3 | 32997112 | missense variant | G/A | snv | 1 | |||
rs754790691 | 1.000 | 0.080 | 3 | 33068890 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs72555370 | 0.925 | 0.120 | 3 | 33072587 | missense variant | G/A | snv | 2.8E-05 | 2.8E-05 | 1 | |
rs35289681 | 1.000 | 0.120 | 3 | 33068891 | missense variant | G/A | snv | 1.8E-02 | 1.6E-02 | 1 | |
rs772155434 | 3 | 33058188 | missense variant | C/T | snv | 4.0E-06 | 1 |