ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.3846C>T (p.Ser1282=)

dbSNP: rs747787010
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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 RCV000928020 SCV001073621 likely benign not provided 2018-09-10 criteria provided, single submitter clinical testing

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