Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3130544 | 0.807 | 0.360 | 6 | 31090563 | intergenic variant | C/A | snv | 7.4E-02 | 10 | ||
rs2857595 | 0.827 | 0.320 | 6 | 31600692 | intergenic variant | G/A | snv | 0.27 | 9 | ||
rs2516400 | 0.827 | 0.320 | 6 | 31513328 | upstream gene variant | G/A | snv | 0.32 | 8 | ||
rs1794282 | 0.807 | 0.320 | 6 | 32698749 | intergenic variant | C/T | snv | 6.4E-02 | 6 | ||
rs3094054 | 0.807 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv | 6 | |||
rs3130473 | 0.882 | 0.160 | 6 | 31231431 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs7762279 | 0.807 | 0.360 | 6 | 32787513 | intergenic variant | T/C | snv | 8.4E-02 | 6 | ||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs3130350 | 0.827 | 0.280 | 6 | 30360062 | upstream gene variant | G/T | snv | 7.1E-02 | 5 | ||
rs2596560 | 0.851 | 0.280 | 6 | 31387541 | intergenic variant | T/C | snv | 0.22 | 4 | ||
rs2844659 | 0.851 | 0.280 | 6 | 30856755 | intergenic variant | C/G;T | snv | 4 | |||
rs3129963 | 0.851 | 0.280 | 6 | 32412431 | downstream gene variant | A/G | snv | 0.17 | 4 | ||
rs2844657 | 0.882 | 0.240 | 6 | 30861745 | upstream gene variant | A/G | snv | 0.17 | 3 | ||
rs3095089 | 0.882 | 0.240 | 6 | 30966017 | upstream gene variant | G/T | snv | 0.16 | 3 | ||
rs3135353 | 0.882 | 0.280 | 6 | 32425100 | intergenic variant | C/T | snv | 9.4E-02 | 3 | ||
rs7749323 | 0.925 | 0.200 | 6 | 137909252 | intergenic variant | G/A | snv | 3.3E-02 | 2 | ||
rs111945767 | 1.000 | 0.120 | 6 | 32549268 | downstream gene variant | G/C | snv | 0.45 | 1 | ||
rs231770 | 1.000 | 0.120 | 2 | 203864430 | upstream gene variant | C/T | snv | 0.42 | 1 | ||
rs4361859 | 1.000 | 0.120 | 9 | 97062415 | regulatory region variant | G/A | snv | 0.77 | 1 | ||
rs8058694 | 1.000 | 0.120 | 16 | 16185006 | missense variant | G/T | snv | 0.42 | 0.43 | 1 | |
rs8058696 | 1.000 | 0.120 | 16 | 16185012 | synonymous variant | G/C;T | snv | 0.42 | 1 | ||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 6 | ||
rs3761389 | 1.000 | 0.120 | 21 | 44285055 | upstream gene variant | G/A | snv | 0.14 | 1 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs2071591 | 0.925 | 0.160 | 6 | 31548022 | intron variant | G/A;C | snv | 2 |