List of variants in gene GCK reported as benign by Genetic Services Laboratory, University of Chicago

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.645C>T (p.Tyr215=)	rs144723656	0.00682
NM_000162.5(GCK):c.31G>A (p.Ala11Thr)	rs116093166	0.00663
NM_000162.5(GCK):c.339C>T (p.Asp113=)	rs149412035	0.00451
NM_000162.5(GCK):c.618G>A (p.Thr206=)	rs142817246	0.00400
NM_000162.5(GCK):c.-215A>G	rs13306390	0.00065
NM_000162.5(GCK):c.9C>T (p.Asp3=)	rs142553382	0.00009

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