Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs1569686 | 0.752 | 0.400 | 20 | 32779273 | intron variant | G/A;C;T | snv | 15 | |||
rs1805010 | 0.752 | 0.400 | 16 | 27344882 | missense variant | A/C;G;T | snv | 0.45 | 12 | ||
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs3130618 | 0.827 | 0.360 | 6 | 31664357 | missense variant | C/A;T | snv | 0.15; 4.0E-06 | 7 | ||
rs3094054 | 0.807 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv | 6 | |||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 6 | |||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs204990 | 0.851 | 0.280 | 6 | 32193653 | intron variant | C/A;T | snv | 4 | |||
rs2844659 | 0.851 | 0.280 | 6 | 30856755 | intergenic variant | C/G;T | snv | 4 | |||
rs1422673 | 0.925 | 0.160 | 5 | 151059427 | intron variant | C/G;T | snv | 2 | |||
rs2071591 | 0.925 | 0.160 | 6 | 31548022 | intron variant | G/A;C | snv | 2 | |||
rs2737713 | 1.000 | 0.120 | 1 | 236537507 | missense variant | T/A | snv | 2 | |||
rs887464 | 0.925 | 0.200 | 6 | 31178143 | intron variant | C/A;T | snv | 2 | |||
rs11466316 | 1.000 | 0.120 | 19 | 41353431 | 5 prime UTR variant | G/A;T | snv | 1 | |||
rs150881176 | 1.000 | 0.120 | 6 | 29979963 | downstream gene variant | T/C | snv | 1 | |||
rs8058696 | 1.000 | 0.120 | 16 | 16185012 | synonymous variant | G/C;T | snv | 0.42 | 1 | ||
rs9963862 | 1.000 | 0.120 | 18 | 23007948 | intron variant | G/A;C | snv | 1 | |||
rs564353179 | 1.000 | 0.120 | 2 | 178780121 | missense variant | C/G | snv | 9.6E-05 | 9.1E-05 | 1 | |
rs11575936 | 0.851 | 0.200 | 6 | 137219288 | missense variant | C/T | snv | 1.3E-03 | 4.1E-04 | 4 | |
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 20 | ||
rs7749323 | 0.925 | 0.200 | 6 | 137909252 | intergenic variant | G/A | snv | 3.3E-02 | 2 | ||
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 16 | |
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs7775397 | 0.790 | 0.400 | 6 | 32293475 | missense variant | T/G | snv | 6.0E-02 | 6.4E-02 | 7 |