ClinVar Miner

List of variants in gene combination FANCD2, LOC107303338 reported as likely benign for Fanconi anemia complementation group D2

Included ClinVar conditions (1):

Fanconi anemia, complementation group D2

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP
NM_033084.5(FANCD2):c.1275C>T (p.Tyr425=)	rs764447374

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