ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.2392C>T (p.Leu798=)

dbSNP: rs1855760265
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002537862 SCV003011303 likely benign not provided 2023-10-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279739 SCV001466860 uncertain significance Autosomal recessive osteopetrosis 1 2020-08-13 no assertion criteria provided clinical testing

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