Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs371194629 | 0.790 | 0.320 | 6 | 29830804 | 3 prime UTR variant | -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT | ins | 8 | |||
rs148735424 | 1.000 | 0.120 | 6 | 32697982 | intergenic variant | -/TTCGTC;TTCGTCAGAC | delins | 1 | |||
rs2069762 | 0.672 | 0.560 | 4 | 122456825 | upstream gene variant | A/C | snv | 0.24 | 23 | ||
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 16 | |
rs2650000 | 0.851 | 0.200 | 12 | 120951159 | intron variant | A/C | snv | 0.70 | 10 | ||
rs316019 | 0.790 | 0.360 | 6 | 160249250 | missense variant | A/C | snv | 0.90 | 0.89 | 8 | |
rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 7 | ||
rs1058026 | 0.925 | 0.120 | 6 | 31353908 | 3 prime UTR variant | A/C | snv | 0.21 | 5 | ||
rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
rs3129871 | 0.827 | 0.320 | 6 | 32438565 | upstream gene variant | A/C | snv | 0.59 | 5 | ||
rs11721827 | 0.851 | 0.200 | 4 | 186069983 | intron variant | A/C | snv | 0.12 | 4 | ||
rs1265564 | 1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 | 4 | ||
rs780229030 | 0.851 | 0.280 | 19 | 45032710 | missense variant | A/C | snv | 4 | |||
rs2234694 | 0.882 | 0.240 | 21 | 31666552 | intron variant | A/C | snv | 3.6E-02 | 3.4E-02 | 3 | |
rs1980495 | 0.925 | 0.160 | 6 | 32379017 | intron variant | A/C | snv | 0.24 | 2 | ||
rs3095340 | 1.000 | 0.120 | 6 | 30759162 | intron variant | A/C | snv | 0.16 | 2 | ||
rs3135002 | 1.000 | 0.120 | 6 | 32700662 | TF binding site variant | A/C | snv | 0.80 | 2 | ||
rs4948088 | 0.925 | 0.160 | 7 | 50959497 | intron variant | A/C | snv | 0.96 | 2 | ||
rs1217385 | 1.000 | 0.120 | 1 | 113875583 | intron variant | A/C | snv | 0.58 | 1 | ||
rs1428168076 | 1.000 | 0.120 | 11 | 34452152 | missense variant | A/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs209473 | 1.000 | 0.120 | 6 | 32955131 | intron variant | A/C | snv | 0.56 | 1 | ||
rs2254193 | 1.000 | 0.120 | 9 | 16801852 | intron variant | A/C | snv | 8.5E-02 | 1 | ||
rs229533 | 1.000 | 0.120 | 22 | 37191071 | intron variant | A/C | snv | 0.50 | 1 | ||
rs439121 | 1.000 | 0.120 | 6 | 33225090 | intergenic variant | A/C | snv | 0.27 | 1 | ||
rs917911 | 1.000 | 0.120 | 12 | 9753255 | 3 prime UTR variant | A/C | snv | 0.29 | 1 |