b23bfd1da3c9926158cd96b7f73bf6b889c3d424 angie Thu Oct 31 14:06:35 2019 -0700 Minor wording tweak, refs #23283 diff --git src/hg/makeDb/trackDb/human/dbSnp153Composite.html src/hg/makeDb/trackDb/human/dbSnp153Composite.html index d74342c..1666146 100644 --- src/hg/makeDb/trackDb/human/dbSnp153Composite.html +++ src/hg/makeDb/trackDb/human/dbSnp153Composite.html @@ -231,39 +231,38 @@ <td class="number">106940656</td> <td class="number">109838613</td> <td>This variant overlaps another variant with a different type/class.</td> </tr> <tr> <td>overlapSameClass</td> <td class="number">16890303</td> <td class="number">17228657</td> <td>This variant overlaps another with the same type/class but different start/end.</td> </tr> <tr> <td>rareAll</td> <td class="number">662571654</td> <td class="number">681626796</td> <td>Variant is "rare", i.e. has a Minor Allele Frequency of less than 1% - in all projects reporting frequencies, or has been reported without frequency data.</td> + in all projects reporting frequencies, or has no frequency data.</td> </tr> <tr> <td>rareSome</td> <td class="number">670927558</td> <td class="number">690089717</td> <td>Variant is "rare", i.e. has a Minor Allele Frequency of less than 1% - in some, but not all, projects reporting frequencies, or has been reported without - frequency data.</td> + in some, but not all, projects reporting frequencies, or has no frequency data.</td> </tr> <tr> <td>revStrand</td> <td class="number">3813390</td> <td class="number">4512600</td> <td>The orientation of the currently viewed reference genome sequence is different from the orientation of dbSNP's preferred top-level assembly sequence; alleles are presented on the forward strand of the currently viewed reference sequence.</td> </tr> </table> <p> while others may indicate that the reference genome contains a rare variant or sequencing issue: </p> <table class="descTbl"> <tr><th>keyword in data file (dbSnp152.bb)</th>