The influence in the variant on RNA or protein perform, determined by experimental evidence from submitters.
This benefit is calculated by NCBI determined by info from submitters. Study our rules for calculating the critique status. The volume of submissions which lead to this review standing is demonstrated in parentheses.
There isn't a useful proof in ClinVar for this variation. When you've got created purposeful details for this variation, make sure you look at distributing that knowledge to ClinVar.
This column incorporates additional information supporting the classification, like citations, the comment on classification, and thorough proof supplied as observations with the variant through the submitter.
The ailment to the classification, supplied by the submitter for this submitted (SCV) history. This column also incorporates the affected status and allele origin of individuals noticed using this variant.
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There are no citations for germline classification of the variant in ClinVar. If you already know of citations for this variation, you should look at distributing that data to ClinVar.
The number of variants in ClinVar that are contained within just this gene, using a link to watch the list of variants.
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The amount of variants in ClinVar for this gene, including smaller variants in the gene and bigger CNVs that overlap or completely comprise the gene.
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Stars symbolize the overview standing, or the extent of overview supporting the submitted (SCV) file. This benefit is calculated by NCBI dependant on data within the submitter.