ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.2106A>G (p.Glu702=)

dbSNP: rs771368616
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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 RCV002069470 SCV002467851 likely benign not provided 2022-08-09 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279732 SCV001466852 uncertain significance Autosomal recessive osteopetrosis 1 2020-04-16 no assertion criteria provided clinical testing

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