ClinVar Miner

Submissions for variant NM_006895.3(HNMT):c.180C>T (p.Gly60=)

gnomAD frequency: 0.00006  dbSNP: rs529181997
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000921131 SCV001066523 benign not provided 2018-04-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000921131 SCV002544070 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing HNMT: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000921131 SCV005245357 benign not provided criteria provided, single submitter not provided

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