List of variants in gene BPGM reported as uncertain significance for anemia

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_001724.5(BPGM):c.461G>A (p.Arg154Gln)
NM_001724.5(BPGM):c.62G>A (p.Arg21His)
NM_001724.5(BPGM):c.679C>T (p.Arg227Cys)

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