ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1996A>C (p.Arg666=)

dbSNP: rs767714758
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 RCV000929295 SCV001074923 likely benign not provided 2023-10-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832105 SCV002094925 likely benign Autosomal recessive osteopetrosis 1 2021-09-13 no assertion criteria provided clinical testing

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