ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1875C>G (p.Leu625=)

gnomAD frequency: 0.00002  dbSNP: rs758830999
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001466445 SCV001670447 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279728 SCV001466847 uncertain significance Autosomal recessive osteopetrosis 1 2020-04-16 no assertion criteria provided clinical testing

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