ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1301G>A (p.Arg434His)

gnomAD frequency: 0.00068  dbSNP: rs150243412
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000518758 SCV000615785 benign not specified 2016-09-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003708536 SCV004485862 likely benign not provided 2024-09-30 criteria provided, single submitter clinical testing

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