List of variants in gene VKORC1 reported as likely benign for hematologic disorder

Minimum submission review status:		Collection method:
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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_024006.6(VKORC1):c.129C>T (p.Cys43=)	rs61742233	0.00401
NM_024006.6(VKORC1):c.106G>T (p.Asp36Tyr)	rs61742245	0.00150
NM_024006.6(VKORC1):c.352G>C (p.Val118Leu)	rs753570105	0.00036
NM_024006.6(VKORC1):c.*243G>A	rs141753512	0.00019

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