Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 3 | |
rs2056626 | 0.882 | 0.080 | 1 | 167451188 | intron variant | T/G | snv | 0.30 | 3 | ||
rs2075800 | 0.776 | 0.440 | 6 | 31810169 | missense variant | C/T | snv | 0.32 | 0.25 | 3 | |
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 3 | |
rs2516398 | 0.882 | 0.200 | 6 | 31513749 | upstream gene variant | G/T | snv | 0.70 | 3 | ||
rs2516399 | 0.925 | 0.120 | 6 | 31513522 | upstream gene variant | A/G | snv | 0.11 | 3 | ||
rs2523477 | 0.925 | 0.080 | 6 | 31392612 | downstream gene variant | T/C | snv | 0.10 | 3 | ||
rs2596480 | 0.925 | 0.120 | 6 | 31458208 | intron variant | C/G;T | snv | 3 | |||
rs2856705 | 0.882 | 0.200 | 6 | 32703179 | downstream gene variant | C/T | snv | 0.11 | 3 | ||
rs3117230 | 0.882 | 0.200 | 6 | 33107858 | upstream gene variant | A/G | snv | 0.28 | 3 | ||
rs3128930 | 0.925 | 0.120 | 6 | 33107889 | upstream gene variant | C/T | snv | 0.31 | 3 | ||
rs3821236 | 0.882 | 0.160 | 2 | 191038032 | intron variant | G/A | snv | 0.25 | 3 | ||
rs4728142 | 0.732 | 0.320 | 7 | 128933913 | upstream gene variant | G/A | snv | 0.38 | 3 | ||
rs479536 | 0.882 | 0.200 | 6 | 32225901 | upstream gene variant | G/A | snv | 5.0E-02 | 3 | ||
rs6941112 | 0.882 | 0.120 | 6 | 31978837 | intron variant | G/A | snv | 0.25 | 3 | ||
rs707939 | 0.851 | 0.200 | 6 | 31758911 | intron variant | C/A | snv | 0.34 | 0.26 | 3 | |
rs9275224 | 0.851 | 0.200 | 6 | 32692101 | TF binding site variant | A/G | snv | 0.53 | 3 | ||
rs9275390 | 0.882 | 0.120 | 6 | 32701379 | downstream gene variant | T/C | snv | 0.30 | 3 | ||
rs987870 | 0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 | 3 | ||
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 2 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 2 | ||
rs11860650 | 0.882 | 0.120 | 16 | 31315385 | intron variant | C/T | snv | 0.14 | 2 | ||
rs12531711 | 0.827 | 0.200 | 7 | 128977412 | intron variant | A/C;G | snv | 2 | |||
rs12540874 | 0.882 | 0.280 | 7 | 50597225 | intron variant | A/C;G | snv | 2 | |||
rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 2 |