Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs76151636 | 0.776 | 0.280 | 13 | 51944145 | missense variant | G/A;T | snv | 4.0E-06; 9.2E-04 | 10 | ||
rs5030849 | 0.851 | 0.280 | 12 | 102852875 | missense variant | C/A;G;T | snv | 2.2E-04 | 6 | ||
rs5030858 | 0.882 | 0.160 | 12 | 102840493 | missense variant | G/A | snv | 7.6E-04 | 9.0E-04 | 4 | |
rs199475663 | 0.925 | 0.120 | 12 | 102866641 | missense variant | C/G;T | snv | 2.0E-05 | 3 | ||
rs5030841 | 0.925 | 0.120 | 12 | 102912816 | missense variant | A/G | snv | 1.2E-04 | 2.0E-04 | 3 | |
rs5030851 | 0.925 | 0.160 | 12 | 102852815 | missense variant | G/A | snv | 1.0E-04 | 1.3E-04 | 3 | |
rs5030853 | 0.925 | 0.120 | 12 | 102851701 | missense variant | C/A | snv | 5.9E-04 | 3.4E-04 | 3 | |
rs5030856 | 0.925 | 0.120 | 12 | 102843676 | missense variant | T/C | snv | 9.9E-05 | 7.7E-05 | 3 | |
rs5030860 | 0.925 | 0.120 | 12 | 102840474 | missense variant | T/C | snv | 3.7E-04 | 2.4E-04 | 3 | |
rs62508588 | 1.000 | 0.120 | 12 | 102852929 | missense variant | C/A;T | snv | 7.6E-05 | 3 | ||
rs62514903 | 0.925 | 0.120 | 12 | 102894812 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs62642937 | 0.925 | 0.120 | 12 | 102843706 | missense variant | G/A | snv | 4.4E-04 | 3.6E-04 | 3 | |
rs62644499 | 0.925 | 0.120 | 12 | 102840472 | missense variant | C/T | snv | 1.1E-04 | 1.1E-04 | 3 | |
rs75193786 | 0.925 | 0.120 | 12 | 102894893 | missense variant | A/C;G;T | snv | 2.7E-04 | 3 | ||
rs76212747 | 0.925 | 0.120 | 12 | 102852923 | missense variant | A/G;T | snv | 4.8E-04; 2.4E-05 | 3 | ||
rs76687508 | 0.925 | 0.120 | 12 | 102852936 | missense variant | G/A | snv | 1.4E-04 | 8.4E-05 | 3 | |
rs796052017 | 0.925 | 0.120 | 12 | 102852922 | missense variant | CA/TG | mnv | 3 | |||
rs1445893088 | 1.000 | 0.120 | 12 | 102840468 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
rs199475567 | 1.000 | 0.120 | 12 | 102912791 | missense variant | C/A;T | snv | 2 | |||
rs199475572 | 1.000 | 0.120 | 12 | 102877475 | missense variant | T/A;C | snv | 2 | |||
rs199475658 | 1.000 | 0.120 | 12 | 102843646 | missense variant | C/G;T | snv | 4.0E-06 | 2 | ||
rs5030843 | 1.000 | 0.120 | 12 | 102866632 | missense variant | C/G;T | snv | 8.0E-06; 9.2E-05 | 2 | ||
rs5030846 | 1.000 | 0.120 | 12 | 102852930 | stop gained | G/A | snv | 4.4E-05 | 4.2E-05 | 2 | |
rs5030847 | 1.000 | 0.120 | 12 | 102852903 | missense variant | G/A;C;T | snv | 2.8E-05; 4.0E-06 | 2 | ||
rs5030859 | 1.000 | 0.120 | 12 | 102840492 | missense variant | C/T | snv | 4.8E-05 | 3.5E-05 | 2 |