ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.6C>T (p.Ser2=)

dbSNP: rs982258436
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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 RCV001460793 SCV001664672 likely benign Fanconi anemia 2023-10-16 criteria provided, single submitter clinical testing

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