Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs9275312 | 0.807 | 0.280 | 6 | 32697951 | intergenic variant | A/G | snv | 0.16 | 6 | ||
rs660895 | 0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 | 6 | ||
rs2858331 | 0.827 | 0.240 | 6 | 32713500 | upstream gene variant | A/G | snv | 0.42 | 5 | ||
rs2395157 | 0.827 | 0.240 | 6 | 32380368 | intron variant | A/G | snv | 0.24 | 5 | ||
rs3892710 | 0.851 | 0.240 | 6 | 32715085 | upstream gene variant | C/T | snv | 0.22 | 4 | ||
rs2395163 | 0.882 | 0.160 | 6 | 32420032 | intergenic variant | T/C | snv | 0.17 | 3 | ||
rs9268542 | 0.851 | 0.280 | 6 | 32416944 | intergenic variant | A/G | snv | 0.35 | 3 | ||
rs9275184 | 0.882 | 0.200 | 6 | 32686937 | regulatory region variant | T/C | snv | 9.1E-02 | 3 | ||
rs9275390 | 0.882 | 0.120 | 6 | 32701379 | downstream gene variant | T/C | snv | 0.30 | 3 | ||
rs6941112 | 0.882 | 0.120 | 6 | 31978837 | intron variant | G/A | snv | 0.25 | 3 | ||
rs12660382 | 0.882 | 0.200 | 6 | 31475546 | intron variant | C/T | snv | 0.19 | 3 | ||
rs2395488 | 0.882 | 0.160 | 6 | 31478132 | non coding transcript exon variant | A/G | snv | 0.34 | 3 | ||
rs2244839 | 0.882 | 0.200 | 6 | 31470591 | non coding transcript exon variant | G/A;T | snv | 3 | |||
rs3916765 | 0.882 | 0.200 | 6 | 32717773 | upstream gene variant | G/A | snv | 8.5E-02 | 3 | ||
rs3763309 | 0.882 | 0.160 | 6 | 32408196 | upstream gene variant | C/A;T | snv | 3 | |||
rs9469220 | 0.827 | 0.160 | 6 | 32690533 | TF binding site variant | G/A | snv | 0.53 | 2 | ||
rs2246618 | 0.882 | 0.160 | 6 | 31511209 | upstream gene variant | C/T | snv | 0.32 | 2 | ||
rs2516424 | 0.925 | 0.160 | 6 | 31480538 | non coding transcript exon variant | A/G | snv | 0.34 | 2 | ||
rs2071286 | 0.752 | 0.280 | 6 | 32212119 | intron variant | C/T | snv | 0.17 | 2 | ||
rs443198 | 0.851 | 0.200 | 6 | 32222629 | synonymous variant | A/G | snv | 0.38 | 0.39 | 2 | |
rs1980495 | 0.925 | 0.160 | 6 | 32379017 | intron variant | A/C | snv | 0.24 | 2 | ||
rs482759 | 1.000 | 0.080 | 6 | 32227240 | upstream gene variant | A/G;T | snv | 1 | |||
rs7454108 | 0.925 | 0.120 | 6 | 32713706 | upstream gene variant | T/C | snv | 9.1E-02 | 1 |