List of variants in gene CBLIF reported as likely pathogenic for anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005142.3(CBLIF):c.137C>T (p.Ser46Leu)	rs121434322	0.00008
NC_000011.9:g.(?_59603261)_(59604844_?)dup
NM_005142.3(CBLIF):c.370+1G>C
NM_005142.3(CBLIF):c.370+83_426del
NM_005142.3(CBLIF):c.395_396delinsAA (p.Phe132Ter)
NM_005142.3(CBLIF):c.661G>A (p.Gly221Arg)	rs1590859406

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