The thr777 Diaries

The outcome on the variant on RNA or protein function, based on experimental evidence from submitters.

This value is calculated by NCBI according to information from submitters. Study our principles for calculating the evaluation status. The volume of submissions which add to this evaluation position is demonstrated in parentheses.

There is no functional proof in ClinVar for this variation. If you have created purposeful details for this variation, be sure to consider publishing that facts to ClinVar.

The worldwide slight allele frequency calculated through the 1000 Genomes Project. The insignificant allele at this site is indicated in parentheses and could be distinctive in the allele represented by this VCV file.

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There won't be any citations for germline classification of the variant in ClinVar. If you recognize of citations for this variation, please think about distributing that info to ClinVar.

The distributing organization for this submitted (SCV) report. This column also contains the SCV accession and Variation variety, the day this SCV 1st appeared in ClinVar, and also the date this SCV was final up-to-date in ClinVar.

These citations are recognized by LitVar utilizing the rs number, so They might include citations for more than one variant at this site. Make sure you critique the LitVar results meticulously for your variant of curiosity. Report past updated May possibly 19, 2024 

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