Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs9349379 | 0.732 | 0.200 | 6 | 12903725 | intron variant | A/G | snv | 0.32 | 19 | ||
rs2383206 | 0.742 | 0.320 | 9 | 22115027 | intron variant | A/G | snv | 0.49 | 17 | ||
rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 15 | ||
rs1761667 | 0.752 | 0.320 | 7 | 80615623 | intron variant | G/A | snv | 0.49 | 12 | ||
rs1466535 | 0.790 | 0.160 | 12 | 57140687 | intron variant | G/A;C | snv | 9 | |||
rs2074192 | 0.827 | 0.160 | X | 15564667 | intron variant | C/T | snv | 0.40 | 9 | ||
rs2026458 | 0.882 | 0.080 | 6 | 12825642 | intron variant | C/T | snv | 0.34 | 6 | ||
rs702553 | 0.882 | 0.160 | 5 | 60440946 | intron variant | A/T | snv | 0.37 | 6 | ||
rs9632884 | 0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv | 6 | |||
rs877087 | 0.882 | 0.080 | 15 | 33582074 | intron variant | T/C;G | snv | 4 | |||
rs879922 | 0.882 | 0.160 | X | 15572684 | intron variant | C/G | snv | 4 | |||
rs12998782 | 0.882 | 0.160 | 2 | 118967804 | intron variant | C/T | snv | 0.19 | 3 | ||
rs650439 | 1.000 | 0.080 | 13 | 33061802 | intron variant | T/A | snv | 0.82 | 0.81 | 3 | |
rs74577862 | 0.882 | 0.080 | 3 | 186843903 | intron variant | G/A | snv | 1.8E-02 | 3 | ||
rs113309773 | 1.000 | 0.080 | 16 | 75398788 | intron variant | -/A;C | ins | 0.51 | 1 | ||
rs200495339 | 1.000 | 0.080 | 19 | 11078623 | intron variant | G/- | delins | 0.12 | 1 | ||
rs259140 | 1.000 | 0.080 | 7 | 89995033 | intron variant | T/G | snv | 0.79 | 1 | ||
rs2876300 | 1.000 | 0.080 | 6 | 12893871 | intron variant | A/C;G | snv | 1 | |||
rs4675095 | 1.000 | 0.080 | 2 | 226787251 | intron variant | A/T | snv | 5.3E-02 | 1 | ||
rs7265169 | 1.000 | 0.080 | 20 | 384103 | intron variant | C/A;T | snv | 1 | |||
rs17128183 | 0.882 | 0.120 | 14 | 55112795 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs11413744 | 1.000 | 0.080 | 4 | 147474132 | intergenic variant | -/T | delins | 0.15 | 1 |