The influence of your variant on RNA or protein function, depending on experimental evidence from submitters.
This benefit is calculated by NCBI dependant on details from submitters. Examine our regulations for calculating the assessment status. The quantity of submissions which contribute to this evaluate position is shown in parentheses.
There isn't a purposeful proof in ClinVar for this variation. Should you have produced practical info for this variation, remember to contemplate submitting that information to ClinVar.
The worldwide minimal allele frequency calculated because of the one thousand Genomes Venture. The minor allele at this place is indicated in parentheses and may be various in the allele represented by this VCV history.
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Examine our procedures for calculating the evaluate standing. This column also includes a link to the submitter’s assertion conditions if furnished, and the collection method.
The submitting Corporation for this submitted (SCV) report. This column also contains the SCV accession and version selection, the date this SCV to start with appeared in ClinVar, plus the date that this SCV was last current in ClinVar.
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The amount of variants in ClinVar for this gene, such as more compact variants in the gene and larger CNVs that overlap or absolutely consist of the gene.
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Stars symbolize the assessment status, or the extent of critique supporting the submitted (SCV) report. This price is calculated by NCBI determined by knowledge from your submitter.