5ccd51414ab1c9cb5a643739583b315c9a6b00be
rhead
  Mon Apr 18 15:53:00 2011 -0700
Changed location of link to dbSNP.
diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html
index 90d2126..74aca29 100644
--- src/hg/htdocs/indexNews.html
+++ src/hg/htdocs/indexNews.html
@@ -21,33 +21,33 @@
                     To receive announcements of new genome 
                     assembly releases, new software features, updates and 
                     training seminars by email, subscribe to the
                     <A HREF="https://lists.soe.ucsc.edu/mailman/listinfo/genome-announce" 
                     TARGET=_blank>genome-announce</A> mailing list.</P>
 
             
             <!-- start news -->
 
             <!-- hg19 snp132 release -->
 		    <P>
                     <FONT FACE="courier" SIZE="3"><B>18 March 2011 - dbSNP 132 Available for hg19</B></FONT>
 		    </P>
                     <P>
                     We are pleased to announce the release of four tracks derived from
-                    dbSNP build 132, available on the human assembly (GRCh37/hg19).
-                    dbSNP build 132 is <a href="http://www.ncbi.nlm.nih.gov/projects/SNP/"
-                    target=_blank>available at NCBI</a>. The new tracks contain
+                    <a href="http://www.ncbi.nlm.nih.gov/projects/SNP/" target=_blank>dbSNP</a>
+                    build 132, available on the human assembly (GRCh37/hg19).
+                    dbSNP build 132 is available at NCBI. The new tracks contain
                     additional annotation data not included in previous dbSNP tracks, 
                     with corresponding coloring and filtering options in the Genome
                     Browser.
                     </P>
                     <P>
                     As for prior builds of dbSNP, there is a track that contains all
                     mappings of reference SNPs to the human assembly; it is now labeled
                     &quot;All SNPs (132)&quot;.  Three new tracks have been added to show
                     interesting and easily defined subsets of dbSNP:
                     </P>
                     <ul>
                     <li> Common SNPs (132): uniquely mapped variants that appear in at
                     least 1% of the population</li>
 
                     <li>Flagged SNPs (132): uniquely mapped variants, excluding Common