Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7085104 | 1.000 | 0.040 | 10 | 102869116 | intron variant | A/G | snv | 0.35 | 2 | ||
rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
rs12244388 | 1.000 | 0.040 | 10 | 102880295 | intron variant | G/A;T | snv | 1 | |||
rs10883795 | 1.000 | 0.040 | 10 | 102894820 | intron variant | T/C | snv | 0.30 | 1 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs7897654 | 1.000 | 0.040 | 10 | 102902701 | intron variant | T/C | snv | 0.30 | 1 | ||
rs11722779 | 1.000 | 0.040 | 4 | 102906331 | 3 prime UTR variant | T/G | snv | 0.58 | 1 | ||
rs4129148 | 1.000 | 0.040 | Y | 1029445 | intergenic variant | C/G;T | snv | 1 | |||
rs55833108 | 1.000 | 0.040 | 10 | 102981826 | intron variant | G/T | snv | 0.14 | 1 | ||
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 5 | ||
rs10786736 | 1.000 | 0.040 | 10 | 103089359 | 3 prime UTR variant | G/C | snv | 9.9E-02 | 1 | ||
rs10883832 | 1.000 | 0.040 | 10 | 103111522 | intron variant | T/G | snv | 8.4E-02 | 1 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 10 | ||
rs11191582 | 1.000 | 0.040 | 10 | 103153896 | intron variant | G/A | snv | 7.7E-02 | 2 | ||
rs12416331 | 1.000 | 0.040 | 10 | 103169157 | intron variant | T/A | snv | 8.4E-02 | 2 | ||
rs10860964 | 1.000 | 0.040 | 12 | 103202677 | intergenic variant | T/C | snv | 0.28 | 1 | ||
rs190474885 | 1.000 | 0.040 | 10 | 103213560 | upstream gene variant | C/T | snv | 1.7E-02 | 1 | ||
rs9554958 | 1.000 | 0.040 | 13 | 103448176 | upstream gene variant | A/G | snv | 0.52 | 1 | ||
rs35559831 | 1.000 | 0.040 | 2 | 103486682 | intergenic variant | G/A;C | snv | 2 | |||
rs4906335 | 0.925 | 0.040 | 14 | 103554804 | intron variant | C/A;G | snv | 2 | |||
rs11597473 | 1.000 | 0.040 | 10 | 103559284 | intron variant | G/C;T | snv | 1 | |||
rs12887734 | 1.000 | 0.040 | 14 | 103580497 | intron variant | G/T | snv | 0.26 | 2 | ||
rs35229468 | 1.000 | 0.040 | 14 | 103585720 | intron variant | C/T | snv | 0.25 | 2 | ||
rs10895475 | 1.000 | 0.040 | 11 | 103593113 | intergenic variant | C/A;T | snv | 1 | |||
rs9879311 | 1.000 | 0.040 | 3 | 10373659 | intron variant | C/A;T | snv | 2 |