ClinVar Miner

Submissions for variant NM_031206.7(LAS1L):c.1788TGATGAAGA[1] (p.596DDE[1])

dbSNP: rs766197666
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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 RCV000871385 SCV001013035 benign Wilson-Turner syndrome 2024-08-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003884770 SCV004699144 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing LAS1L: BS2

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