ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.10122C>T (p.Ala3374=)

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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 RCV003734434 SCV004536566 likely benign not provided 2022-11-08 criteria provided, single submitter clinical testing

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