Variants in gene GCK with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.-455A>G	rs140894490	0.00101
NM_000162.5(GCK):c.*11C>T	rs200698755	0.00046
NM_000162.5(GCK):c.-17C>T	rs190731555	0.00017
NM_000162.5(GCK):c.735G>A (p.Glu245=)	rs775481896	0.00016
NM_000162.5(GCK):c.364-13G>A	rs372405219	0.00015
NM_000162.5(GCK):c.213C>T (p.Val71=)	rs143128547	0.00014
NM_000162.5(GCK):c.1288C>T (p.Leu430=)	rs193922276	0.00013
NM_000162.5(GCK):c.363+9C>T	rs200985182	0.00011
NM_000162.5(GCK):c.363+6C>A	rs751756042	0.00004
NM_000162.5(GCK):c.198A>G (p.Pro66=)	rs377410513	0.00003
NM_000162.5(GCK):c.-452G>A	rs187173652	0.00002
NM_000162.5(GCK):c.680-14G>C	rs577968084
NM_000162.5(GCK):c.680-19C>T
NM_000162.5(GCK):c.835G>C (p.Glu279Gln)	rs104894005
NM_000162.5(GCK):c.852C>G (p.Pro284=)

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