ClinVar Miner

Submissions for variant NM_001146.5(ANGPT1):c.228G>A (p.Pro76=)

dbSNP: rs147086219
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000966204 SCV001113497 benign not provided 2024-01-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000966204 SCV005267923 benign not provided criteria provided, single submitter not provided
Clinical Genetics, Academic Medical Center RCV001701386 SCV001921767 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001701386 SCV001926334 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000966204 SCV001980154 likely benign not provided no assertion criteria provided clinical testing

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