List of variants in gene KLKB1 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000892.5(KLKB1):c.428G>A (p.Ser143Asn)	rs3733402	0.59489
NM_000892.5(KLKB1):c.808A>G (p.Thr270Ala)	rs113884104	0.00344

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