Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs148735424 | 1.000 | 0.120 | 6 | 32697982 | intergenic variant | -/TTCGTC;TTCGTCAGAC | delins | 1 | |||
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 11 | |
rs2650000 | 0.851 | 0.200 | 12 | 120951159 | intron variant | A/C | snv | 0.70 | 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 | ||
rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 5 | ||
rs1980495 | 0.925 | 0.160 | 6 | 32379017 | intron variant | A/C | snv | 0.24 | 2 | ||
rs4948088 | 0.925 | 0.160 | 7 | 50959497 | intron variant | A/C | snv | 0.96 | 2 | ||
rs1265564 | 1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 | 1 | ||
rs2069762 | 0.672 | 0.560 | 4 | 122456825 | upstream gene variant | A/C | snv | 0.24 | 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 | ||
rs3095340 | 1.000 | 0.120 | 6 | 30759162 | intron variant | A/C | snv | 0.16 | 1 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 2 | ||
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 2 | ||
rs241425 | 0.925 | 0.160 | 6 | 32837132 | intron variant | A/C;G | snv | 2 | |||
rs10770141 | 1.000 | 0.120 | 11 | 2172610 | upstream gene variant | A/C;G | snv | 1 | |||
rs3957148 | 0.925 | 0.160 | 6 | 32714360 | upstream gene variant | A/C;G | snv | 0.10 | 1 | ||
rs3134603 | 0.851 | 0.360 | 6 | 32158225 | non coding transcript exon variant | A/C;G;T | snv | 4 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
rs3094061 | 0.925 | 0.160 | 6 | 30353412 | downstream gene variant | A/C;T | snv | 2 | |||
rs3094682 | 1.000 | 0.120 | 6 | 31296684 | intron variant | A/C;T | snv | 1 |