ClinVar Miner

Submissions for variant NM_024582.4(FAT4):c.3402A>T (p.Glu1134Asp) (rs144768563)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000908699 SCV000526852 benign not provided 2019-05-17 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24074368)
Invitae RCV000908699 SCV001053476 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000908699 SCV001809317 uncertain significance not provided no assertion criteria provided clinical testing

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