ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.844-10_844-8del

dbSNP: rs758617953
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000206232 SCV000259259 likely benign Fanconi anemia 2024-01-25 criteria provided, single submitter clinical testing
Counsyl RCV000670094 SCV000794910 uncertain significance Fanconi anemia complementation group C 2017-10-19 criteria provided, single submitter clinical testing
Mendelics RCV000988210 SCV001137847 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing

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