f286e5c10c6344503cf9cd73d594070b5f22a671
max
  Wed Feb 23 03:13:57 2022 -0800
adding the new links that ClinVar added a few months ago to our hgc page, refs #28926

diff --git src/hg/utils/otto/clinvar/clinvar.as src/hg/utils/otto/clinvar/clinvar.as
index 17da1a4..d66aeb9 100644
--- src/hg/utils/otto/clinvar/clinvar.as
+++ src/hg/utils/otto/clinvar/clinvar.as
@@ -21,25 +21,25 @@
     string molConseq;         "Molecular Consequence"
     string snpId;         "dbSNP ID"
     string nsvId;         "dbVar ID"
     lstring rcvAcc;         "ClinVar Allele Submission"
     string testedInGtr;         "Genetic Testing Registry"
     lstring phenotypeList;         "Phenotypes"
     lstring phenotype;         "Phenotype identifiers"
     string origin;         "Allele origin"
     string assembly;         "Genome assembly"
     string cytogenetic;         "Cytogenetic status"
     lstring _jsonHgvsTable;         "HGVS names"
     lstring _hgvsProt;         "Protein HGVS"
     string numSubmit;         "Number of submitters"
     string lastEval;         "Last evaluation"
     string guidelines;         "Guidelines"
-    lstring otherIds;         "Other identifiers e.g. OMIM IDs, etc."
+    lstring otherIds;         "Other identifiers (ClinGen, OMIM, etc.)"
     lstring _mouseOver;        "Mouse over text"
     string _clinSignCode;        "Clinical Significance"
     string _originCode;        "Allele Origin Code"
     string _allTypeCode;        "Variation Type"
     uint _varLen;            "Variant Length in base pairs"
     uint _starCount;         "Number of stars"
     int _variantId;           "ClinVar variant ID"
     string _dbVarSsvId;           "dbVar SSV ID"
     )