8999273deebb9514bab0282c96011acb4355ecbd
angie
  Fri May 17 13:25:31 2019 -0700
Simplifying hgVai documentation disclaimer that it's not for medical use.

diff --git src/hg/htdocs/goldenPath/help/hgVaiHelpText.html src/hg/htdocs/goldenPath/help/hgVaiHelpText.html
index 1be1752..74941d8 100755
--- src/hg/htdocs/goldenPath/help/hgVaiHelpText.html
+++ src/hg/htdocs/goldenPath/help/hgVaiHelpText.html
@@ -14,32 +14,31 @@
 types of relevant information: the dbSNP identifier if the variant
 is found in
 <A HREF="https://www.ncbi.nlm.nih.gov/projects/SNP/"
 TARGET=_BLANK>dbSNP</A>,
 protein damage scores for missense variants from the
 <A HREF="https://sites.google.com/site/jpopgen/dbNSFP"
 TARGET=_BLANK>Database of Non-synonymous Functional Predictions (dbNSFP)</A>,
 and conservation scores computed from multi-species alignments.
 The VAI can optionally filter results to retain only specific functional
 effect categories, variant properties and multi-species conservation status.
 </P>
 
 <div class='warn-note' style='border: 2px solid #9e5900; padding: 5px 20px;
      background-color: #ffe9cc;'>
 <p><span style='font-weight: bold; color: #c70000;'>NOTE:</span><br>
-The VAI is only a research tool, meant to be used by those who have been
-properly trained in the interpretation of genetic data,
+The VAI is only a research tool
 and should never be used to make any kind of medical decision.
 We urge users seeking information about a personal medical or genetic
 condition to consult with a qualified physician for diagnosis and for
 answers to personal questions.
 </p></div><BR>
 
 <a name="variantCalls"></a>
 <h2>Submitting your variant calls</h2>
 <P>
 In order to use the VAI, you must provide variant calls in either the
 <A HREF="../../FAQ/FAQformat.html#format10" TARGET=_BLANK>Personal Genome SNP (pgSnp)</A> or
 <A HREF="../help/vcf.html" TARGET=_BLANK>VCF</A> format.
 pgSnp-formatted variants may be uploaded as a
 <A HREF="../help/hgTracksHelp.html#CustomTracks"
 TARGET=_BLANK>Custom Track</A>.