ClinVar Miner

Submissions for variant NM_001174089.2(SLC4A11):c.2043C>T (p.His681=)

dbSNP: rs2122510584
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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 RCV001458129 SCV001661944 likely benign not provided 2020-10-30 criteria provided, single submitter clinical testing

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