7256393cc0ec2ff7f9a2c3322c69ccf39b99e4db max Fri Feb 9 09:51:55 2024 -0800 dbsnp label change, refs #32901 diff --git src/hg/lib/bigDbSnp.c src/hg/lib/bigDbSnp.c index 62b7548..7c2ecc1 100644 --- src/hg/lib/bigDbSnp.c +++ src/hg/lib/bigDbSnp.c @@ -315,31 +315,31 @@ "Variant is in ClinVar." }, { bdsClinvarBenign, "Variant is in ClinVar with clinical significance of benign and/or likely benign." }, { bdsClinvarConflicting, "Variant is in ClinVar with reports of both benign and pathogenic significance." }, { bdsClinvarPathogenic, "Variant is in ClinVar with clinical significance of pathogenic and/or likely pathogenic." }, { bdsClusterError, "This variant has the same start, end and class as another variant; " "they probably should have been merged into one variant." }, { bdsCommonAll, "Variant is \"common\", i.e. has a Minor Allele Frequency of at least 1% " "in all projects reporting frequencies." }, { bdsCommonSome, "Variant is \"common\", i.e. has a Minor Allele Frequency of at least 1% " - "in some, but not all, projects reporting frequencies." }, + "in some, but not all, projects reporting frequencies. This is not the same as the Common dbSNP data, which is only comprised of variants from 1000 Genomes Phase 3 that have a MAF >= 1%" }, { bdsDiffMajor, "Different frequency sources have different major alleles " "(see table of allele frequencies above)." }, { bdsFreqIncomplete, "At least one project's frequency data is incomplete (only one allele reported)." }, { bdsFreqIsAmbiguous, "At least one allele reported by at least one project " "contains an IUPAC ambiguous base (e.g. 'R' for 'A or G')." }, { bdsFreqNotMapped, "At least one project reported frequencies on a different assembly, for which dbSNP does not " "provide a mapping. The mapping on this assembly may have an issue." }, { bdsFreqNotRefAlt, "The reference genome allele is not the major allele in at least one project." }, { bdsMultiMap, "This variant has been mapped to more than one distinct genomic location." },