List of variants in gene GCK reported as likely benign for Permanent neonatal diabetes mellitus

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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: 11

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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.*92C>A	rs557990162	0.00389
NM_000162.5(GCK):c.46-12C>T	rs142829768	0.00296
NM_000162.5(GCK):c.209-8G>A	rs144798843	0.00249
NM_000162.5(GCK):c.*356G>A	rs146107173	0.00247
NM_000162.5(GCK):c.333C>T (p.Pro111=)	rs61736250	0.00235
NM_000162.5(GCK):c.208+11G>A	rs77440690	0.00124
NM_000162.5(GCK):c.*510C>T	rs141645300	0.00050
NM_000162.5(GCK):c.*735C>A	rs556996030	0.00038
NM_000162.5(GCK):c.-452G>A	rs187173652	0.00002
NM_000162.5(GCK):c.*297T>G	rs527259972	0.00001

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