ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1135-25G>A (rs201770712)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mendelics	RCV000987096	SCV001136294	benign	Fanconi anemia, complementation group A	2019-05-28	criteria provided, single submitter	clinical testing

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