ClinVar Miner

List of variants studied for Fanconi anemia complementation group D2 by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (1):

Fanconi anemia, complementation group D2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

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HGVS	dbSNP
NM_033084.5(FANCD2):c.1348A>G (p.Ile450Val)	rs145129959
NM_033084.5(FANCD2):c.1777C>T (p.Pro593Ser)	rs147523071
NM_033084.5(FANCD2):c.2803A>C (p.Ile935Leu)	rs61751578
NM_033084.5(FANCD2):c.28T>C (p.Ser10Pro)	rs150075366
NM_033084.5(FANCD2):c.310A>G (p.Ile104Val)	rs774299094

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