ClinVar Miner

List of variants in gene FANCD2 reported as likely pathogenic for Fanconi anemia complementation group D2

Included ClinVar conditions (1):

Fanconi anemia, complementation group D2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP
NM_001018115.3(FANCD2):c.3095del (p.Asn1032fs)	rs1559399574
NM_001018115.3(FANCD2):c.39dup (p.Glu14fs)	rs1575723664

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