List of variants in gene HK3 reported as benign for not provided

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_002115.3(HK3):c.2187C>T (p.Thr729=)	rs35676647	0.02436
NM_002115.3(HK3):c.218G>A (p.Arg73Gln)	rs61739890	0.01104
NM_002115.3(HK3):c.708G>A (p.Pro236=)	rs112160979	0.00541
NM_002115.3(HK3):c.2198C>G (p.Ala733Gly)	rs78805667	0.00381

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