ClinVar Miner

Submissions for variant NM_004415.4(DSP):c.1695C>T (p.Ile565=) (rs752714010)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000620376 SCV000736930 likely benign Cardiovascular phenotype 2017-09-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000772657 SCV000905916 likely benign Cardiomyopathy 2018-09-17 criteria provided, single submitter clinical testing

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