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Merge pull request #141 from griffithlab/obigriffith-patch-1
Update origin.rst
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docs/model/evidence/origin.rst

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@@ -36,6 +36,9 @@ Population frequencies should be based on current population databases (e.g., gn
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* - Common Germline
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- |signal|
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- Defined as variants with >1% allele frequency in the population relevant to the publication where the evidence is derived. Are welcome in CIViC, however, generally considered low priority for curation efforts.
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* - Combined
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- ||
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- Variants in the corresponding Complex Molecular Profile have heterogeneous/multiple origins.
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* - Unknown
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- |question-circle|
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- May be used in instances where the publication is ambiguous about the origin of the variant although ordinarily an origin would be known (e.g., tumor-only analysis, analyses including both germline and somatic variants).

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