ClinVar Miner

Submissions for variant NM_153218.4(LACC1):c.112A>G (p.Lys38Glu)

gnomAD frequency: 0.00488  dbSNP: rs34414396
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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 RCV000894519 SCV001038505 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000894519 SCV003917283 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing LACC1: BP4, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000894519 SCV005230225 benign not provided criteria provided, single submitter not provided

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