ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.849+7C>G (rs370740228)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000156311 SCV000206029 likely benign not specified 2014-01-30 criteria provided, single submitter clinical testing 849+7C>G in intron 8 of MYO7A: This variant is not expected to have clinical sig nificance because it is not located within the splice consensus sequence and is not predicted to alter splicing.
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000724827 SCV000232498 uncertain significance not provided 2015-05-19 criteria provided, single submitter clinical testing
Invitae RCV000724827 SCV001073900 likely benign not provided 2020-12-06 criteria provided, single submitter clinical testing

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