ClinVar Miner

Submissions for variant NM_004415.4(DSP):c.939+13dup (rs730880360)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000156256 SCV000205972 likely benign not specified 2013-12-05 criteria provided, single submitter clinical testing 939+13_939+14insC in intron 7 of DSP: This variant is not expected to have clini cal significance because it is not located within the splice consensus sequence. 939+13_939+14insC in intron 7 of DSP (allele frequency = n/a)

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