List of variants in gene CBLIF reported as not provided for hereditary intrinsic factor deficiency

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005142.2(CBLIF):c.-376A>T	rs796064509
NM_005142.3(CBLIF):c.346C>T (p.Gln116Ter)	rs796064508
NM_005142.3(CBLIF):c.432GAA[1] (p.Lys145del)	rs770530971

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