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Human Variation: Annotation and Submit Batch Data with Clinical Impact

Submit multiple variants using HGVS nomenclature with an opportunity to identify their clinical relevance
This dbSNP submission page will be retired by December 1, 2015 and can no longer be used to submit data to ClinVar. Please submit your clinically relevant variants directly to ClinVar; and use the Variation Reporter site to search by HGVS expressions.

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