List of variants in gene PKLR reported as likely 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.1516G>A (p.Val506Ile)	rs8177988	0.00414
NM_000298.6(PKLR):c.181C>T (p.Leu61=)	rs8177962	0.00289
NM_000298.6(PKLR):c.1686C>T (p.Ser562=)	rs140859641	0.00040
NM_000298.6(PKLR):c.375+10G>T	rs8177971

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