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You must be logged in to vote 🙏 Best practice for representing a subset of variants (e.g., pathogenic variants) from a gene?
enhancementNew feature or request questionFurther information is requested -
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You must be logged in to vote 🙏 Selecting the correct
help wantedDefiningAllelefor a Canonical Variant in ClinvarExtra attention is needed questionFurther information is requested -
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You must be logged in to vote 🙏 Shouldn't CategoricalCnv be based on a CanonicalLocation vs a Contextual Location?
help wantedExtra attention is needed questionFurther information is requested decision-record