ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group D2 by Leiden Open Variation Database

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: 4

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HGVS	dbSNP
NM_001018115.3(FANCD2):c.1278+6T>C	rs0
NM_001018115.3(FANCD2):c.1279G>T (p.Val427Phe)	rs0
NM_001018115.3(FANCD2):c.3802T>G (p.Trp1268Gly)	rs0
NM_033084.5(FANCD2):c.491+1G>A	rs943009372

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