Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75961395 | 0.763 | 0.280 | 7 | 117509123 | missense variant | G/A;T | snv | 4.0E-05 | 10 | ||
rs77932196 | 0.790 | 0.280 | 7 | 117540270 | missense variant | G/A;C;T | snv | 2.4E-05; 2.4E-05 | 8 | ||
rs786205866 | 0.807 | 0.160 | 20 | 63495062 | missense variant | C/T | snv | 7 | |||
rs6190 | 0.827 | 0.120 | 5 | 143400772 | missense variant | C/G;T | snv | 4.0E-06; 1.8E-02 | 6 | ||
rs142920240 | 0.851 | 0.240 | 7 | 117540273 | missense variant | T/A | snv | 1.4E-04 | 7.0E-05 | 5 | |
rs104893755 | 0.851 | 0.200 | 3 | 87259959 | missense variant | G/A | snv | 5 | |||
rs137853220 | 0.882 | 0.200 | 17 | 63917909 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs557914261 | 0.925 | 0.160 | 19 | 40458393 | missense variant | G/A | snv | 2.8E-05 | 3 | ||
rs1253103806 | 1.000 | 0.040 | 15 | 98891384 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
rs1218653273 | 0.925 | 0.160 | 17 | 42292005 | missense variant | C/T | snv | 4.0E-06 | 3 |