ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1119C>T (p.Gly373=)

dbSNP: rs759279602
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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 RCV001456155 SCV001659931 likely benign not provided 2021-05-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279337 SCV001466425 uncertain significance Autosomal recessive osteopetrosis 1 2020-04-15 no assertion criteria provided clinical testing

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