ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2632_2633delinsCG (p.Glu878Arg)

dbSNP: rs2039079300
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001330800 SCV001522613 uncertain significance Fanconi anemia complementation group A 2019-08-09 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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