ClinVar Miner

List of variants reported as benign for Fanconi anemia complementation group D2 by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Included ClinVar conditions (1):

Fanconi anemia complementation group D2

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.1278+3_1278+5del	rs375350046
NM_001018115.3(FANCD2):c.1401G>A (p.Thr467=)	rs12330369

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