Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1358030 | 0.925 | 0.120 | 10 | 106363841 | intergenic variant | G/A | snv | 0.57 | 2 | ||
rs7111341 | 0.925 | 0.120 | 11 | 2191936 | regulatory region variant | C/T | snv | 0.29 | 2 | ||
rs777334819 | 0.925 | 0.120 | 3 | 12379856 | missense variant | G/A | snv | 3.6E-05 | 2.1E-05 | 2 | |
rs8192556 | 0.925 | 0.120 | 2 | 181678271 | missense variant | G/T | snv | 1.9E-02 | 1.6E-02 | 2 | |
rs7202877 | 0.882 | 0.160 | 16 | 75213347 | intergenic variant | T/C;G | snv | 3 | |||
rs9273368 | 0.882 | 0.120 | 6 | 32658698 | upstream gene variant | G/A | snv | 0.23 | 3 | ||
rs1131580 | 0.882 | 0.160 | 3 | 172505830 | 3 prime UTR variant | A/C;G;T | snv | 4 | |||
rs1801262 | 0.882 | 0.120 | 2 | 181678728 | missense variant | T/C | snv | 0.70 | 0.68 | 4 | |
rs1205538057 | 0.827 | 0.200 | 17 | 63483937 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs4866 | 0.827 | 0.240 | 7 | 2249951 | missense variant | G/A | snv | 2.2E-02 | 1.8E-02 | 5 | |
rs762890235 | 0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 | 5 | |
rs137853236 | 0.807 | 0.280 | 12 | 120997504 | missense variant | C/T | snv | 1.2E-05 | 6 | ||
rs1555212014 | 0.807 | 0.280 | 12 | 120994264 | missense variant | C/T | snv | 6 | |||
rs5435 | 0.851 | 0.200 | 17 | 7283804 | missense variant | T/A;C | snv | 0.65 | 6 | ||
rs754729248 | 0.807 | 0.280 | 12 | 120996568 | missense variant | C/A;G;T | snv | 2.4E-05; 1.9E-04; 3.6E-05 | 6 | ||
rs759853 | 0.827 | 0.320 | 7 | 134459206 | non coding transcript exon variant | G/A | snv | 0.33 | 6 | ||
rs769985775 | 0.851 | 0.160 | X | 32448630 | synonymous variant | T/C | snv | 5.7E-06 | 9.5E-06 | 6 | |
rs11154178 | 0.807 | 0.240 | 6 | 123540174 | intron variant | T/A;C | snv | 7 | |||
rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
rs1800783 | 0.827 | 0.280 | 7 | 150992309 | intron variant | A/C;G;T | snv | 7 | |||
rs1801483 | 0.851 | 0.160 | 17 | 81809839 | missense variant | G/A | snv | 7.4E-03 | 6.3E-03 | 7 | |
rs2260000 | 0.851 | 0.200 | 6 | 31625699 | intron variant | A/G | snv | 0.29 | 7 | ||
rs28485846 | 0.807 | 0.240 | 8 | 35265058 | intron variant | C/T | snv | 5.1E-02 | 7 | ||
rs3761980 | 0.807 | 0.240 | 6 | 36026129 | upstream gene variant | A/G | snv | 0.14 | 7 | ||
rs6910071 | 0.790 | 0.320 | 6 | 32315077 | intron variant | A/G | snv | 0.14 | 7 |