List of variants in gene KLKB1 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000892.5(KLKB1):c.772C>T (p.Leu258Phe)	rs146650319	0.00061
NM_000892.5(KLKB1):c.-2+1G>C	rs954965096

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