ClinVar Miner

Submissions for variant NM_006946.4(SPTBN2):c.3174A>G (p.Glu1058=)

dbSNP: rs1590936888
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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 RCV000982678 SCV001130695 likely benign not provided 2019-02-14 criteria provided, single submitter clinical testing

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