ClinVar Miner

Submissions for variant NM_002204.4(ITGA3):c.1113A>T (p.Leu371Phe)

gnomAD frequency: 0.01568  dbSNP: rs61730085
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000965387 SCV001112653 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
GeneDx RCV000965387 SCV001803336 likely benign not provided 2024-05-16 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Breakthrough Genomics, Breakthrough Genomics RCV000965387 SCV005218090 likely benign not provided criteria provided, single submitter not provided

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