8fa777e7a626753ecf40a7471999dba3a984e272
max
  Tue Apr 21 09:21:39 2020 -0700
more clinvar improvements, refs #24850

diff --git src/hg/makeDb/trackDb/human/trackDb.clinvarTest.ra src/hg/makeDb/trackDb/human/trackDb.clinvarTest.ra
index 8297bff..f7d2525 100644
--- src/hg/makeDb/trackDb/human/trackDb.clinvarTest.ra
+++ src/hg/makeDb/trackDb/human/trackDb.clinvarTest.ra
@@ -1,25 +1,26 @@
 track clinvar
 compositeTrack on
 shortLabel ClinVar Variants
 longLabel ClinVar Variants
 group phenDis
 visibility hide
 type bed 12 +
 itemRgb on
 urls rcvAcc="https://www.ncbi.nlm.nih.gov/clinvar/$$/" geneId="https://www.ncbi.nlm.nih.gov/gene/$$" snpId="https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=$$" nsvId="https://www.ncbi.nlm.nih.gov/dbvar/variants/$$/" origName="https://www.ncbi.nlm.nih.gov/clinvar/variation/$$/"
-scoreLabel ClinVar Star-Rating (0-4)
+#scoreLabel ClinVar Star-Rating (0-4)
+noScoreFilter on
 
     track clinvarMain
     shortLabel ClinVar Short Variants
     longLabel ClinVar Short Variants <= 100bp
     visibility pack
     parent clinvar
     priority 1
     type bigBed 12 +
     filterValues._clinSignCode BN|benign,LB|likely benign,CF|conflicting,PG|pathogenic,LP|likely pathogenic,UC|uncertain,OT|other
     filterType._clinSignCode singleList
     filterValues._originCode GERM|germline,SOM|somatic,GERMSOM|germline/somatic,NOVO|de novo,UNK|unknown
     filterType._originCode singleList
     filterValues._allTypeCode SNV|single nucleotide variant,INS|insertion,DEL|deletion,INDEL|insertion-deletion,dupl|duplication,OTH|other
     filterType._allTypeCode singleList
     filterByRange._valLen on