ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.672C>T (p.Asn224=)

dbSNP: rs774051315
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001452319 SCV001655977 likely benign Fanconi anemia 2020-06-24 criteria provided, single submitter clinical testing

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