ClinVar Miner

Submissions for variant NM_002204.4(ITGA3):c.2920-12T>C

gnomAD frequency: 0.01323  dbSNP: rs60377725
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001550195 SCV001770488 likely benign not provided 2020-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001550195 SCV002451958 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001550195 SCV005218105 likely benign not provided criteria provided, single submitter not provided

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