ClinVar Miner

Submissions for variant NM_033084.5(FANCD2):c.1278+3_1278+5del (rs375350046)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen	RCV000600750	SCV000734236	benign	Fanconi anemia, complementation group D2		no assertion criteria provided	clinical testing

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