List of variants in gene PKLR reported as benign for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000298.6(PKLR):c.*267C>T	rs932972	0.35051
NM_000298.6(PKLR):c.1705C>A (p.Arg569=)	rs1052176	0.35034
NM_000298.6(PKLR):c.*13T>C	rs1052177
NM_000298.6(PKLR):c.375+10G>T	rs8177971

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