ClinVar Miner

Submissions for variant NM_207361.6(FREM2):c.7520-5dup

dbSNP: rs36084034
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000174964 SCV000226372 benign not specified 2014-11-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002054061 SCV002404866 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500470 SCV002808342 likely benign Isolated cryptophthalmia; Fraser syndrome 2 2022-05-23 criteria provided, single submitter clinical testing

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