ClinVar Miner

Submissions for variant NM_002286.6(LAG3):c.58+7C>T

gnomAD frequency: 0.00404  dbSNP: rs183549619
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 RCV000971929 SCV001119608 benign not provided 2018-08-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000971929 SCV005330244 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing LAG3: BP4, BS2

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