ca48d17f1e4bc1e975c84fd3bf3cf18d0d59f577
jnavarr5
  Tue Aug 18 14:38:25 2026 -0700
Implementing Lou's suggestion from code review, refs #38138

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index e2a0d82b51b..901a4a30d7e 100644
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -56,32 +56,32 @@
 <p>Smaller software changes are not announced here.  A summary of the three-weekly release changes can be 
 found <a target=_blank href="https://genecats.gi.ucsc.edu/builds/versions.html">here</a>. 
 For the full list of our daily code changes head to our <a
 href="https://github.com/ucscGenomeBrowser/kent/commits/master"
 target=_blank>GitHub page</a>. Lastly, see our <a href="credits.html" target="_blank">
 credits page</a> for acknowledgments of the data we host.</p>
 
 <!-- ============= 2026 archived news ============= -->
 
 <a name="2026"></a>
 
 <a name="081126"></a>
 <h2>Aug. 11, 2026 &nbsp;&nbsp; Deleteriousness Predictions: ClinPred for hg19 and hg38</h2>
 <p>
 We are pleased to announce the release of the ClinPred pathogenicity score track for
-<a href="/cgi-bin/hgTrackUi?db=hg19&g=clinPred" target="_blank">hg19</a> and
-<a href="/cgi-bin/hgTrackUi?db=hg38&g=clinPred" target="_blank">hg38</a>.
+<a href="/cgi-bin/hgTrackUi?db=hg19&g=clinPred&position=default" target="_blank">hg19</a> and
+<a href="/cgi-bin/hgTrackUi?db=hg38&g=clinPred&position=default" target="_blank">hg38</a>.
 ClinPred is a machine-learning predictor of pathogenicity for nonsynonymous (missense)
 single-nucleotide variants, combining existing pathogenicity scores with population allele
 frequency from gnomAD. It was trained on confidently annotated disease-causing and benign
 variants from ClinVar. Pre-computed scores are provided for all possible human missense
 variants in the exome.
 </p>
 
 <p>
 Scores range from 0 to 1, with higher values indicating a greater predicted likelihood
 that a variant is disease-relevant. The authors recommend a score of &ge; 0.5 as evidence
 of pathogenicity. As with any pathogenicity prediction score, ClinPred is intended as
 supporting evidence rather than a stand-alone classifier.
 </p>
 
 <p>