Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894409 | 0.827 | 0.120 | 13 | 20189332 | missense variant | C/A;G;T | snv | 1.6E-05; 3.6E-05; 4.0E-06 | 6 | ||
rs111033437 | 0.882 | 0.120 | 11 | 77179925 | missense variant | G/A;T | snv | 6 | |||
rs28938175 | 0.851 | 0.120 | 14 | 30877640 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs796053353 | 0.882 | 0.120 | 9 | 127661192 | missense variant | C/T | snv | 6 | |||
rs1057518895 | 1.000 | 0.120 | X | 130137134 | start lost | A/G | snv | 4 | |||
rs121912557 | 0.882 | 0.120 | 6 | 75857198 | missense variant | G/A | snv | 4 | |||
rs758723288 | 0.882 | 0.120 | 10 | 133370686 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 4 | |
rs772606235 | 0.882 | 0.120 | 11 | 121137586 | missense variant | G/A;T | snv | 5.2E-05 | 4 | ||
rs1176235580 | 0.925 | 0.120 | 6 | 73482214 | missense variant | G/A | snv | 3 | |||
rs121908930 | 0.925 | 0.120 | 14 | 30878897 | missense variant | T/A;C | snv | 4.0E-06 | 3 | ||
rs1302739538 | 0.882 | 0.120 | 13 | 20189066 | stop gained | C/G;T | snv | 3 | |||
rs139449947 | 0.925 | 0.120 | 6 | 73482463 | missense variant | G/A | snv | 9.6E-05 | 9.8E-05 | 3 | |
rs144948296 | 0.925 | 0.120 | 15 | 43604750 | stop gained | G/A;C | snv | 1.8E-04 | 3 | ||
rs1471362858 | 0.882 | 0.120 | 6 | 133462408 | missense variant | G/C | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs111033196 | 1.000 | 0.120 | 13 | 20189202 | missense variant | C/A;T | snv | 2.8E-04; 1.4E-02 | 2 | ||
rs11928865 | 1.000 | 0.120 | 3 | 7114015 | intron variant | T/A;G | snv | 2 | |||
rs121909063 | 0.925 | 0.120 | 11 | 121168135 | missense variant | C/A;T | snv | 2 | |||
rs1233562246 | 0.925 | 0.120 | 12 | 80255055 | frameshift variant | T/- | del | 2 | |||
rs1291519904 | 0.925 | 0.120 | 13 | 20189325 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs1323852277 | 0.925 | 0.120 | 4 | 6301903 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1391331735 | 0.925 | 0.120 | 17 | 18126795 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs142668478 | 0.925 | 0.120 | 4 | 6301849 | missense variant | G/A;C;T | snv | 1.8E-04; 4.0E-06 | 2 | ||
rs28937893 | 0.925 | 0.120 | 4 | 6301941 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 2 | ||
rs35725509 | 0.925 | 0.120 | 12 | 82896304 | missense variant | G/A | snv | 1.0E-02 | 6.2E-03 | 2 | |
rs372466080 | 0.925 | 0.120 | 17 | 18166434 | synonymous variant | C/T | snv | 1.9E-04 | 1.0E-04 | 2 |