ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.7644+8T>G

dbSNP: rs2154117770
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001437063 SCV001639909 likely benign Nemaline myopathy 2 2020-06-15 criteria provided, single submitter clinical testing

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