List of variants in gene GCK reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.209-8G>A	rs144798843	0.00249
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.483+8G>A	rs151002306	0.00007
NM_000162.5(GCK):c.600G>A (p.Val200=)	rs773561406	0.00006
NM_000162.5(GCK):c.834C>T (p.Asp278=)	rs200071687	0.00004
NM_000162.5(GCK):c.138G>A (p.Arg46=)	rs550111033	0.00003
NM_000162.5(GCK):c.129C>T (p.Arg43=)	rs760912915	0.00001
NM_000162.5(GCK):c.609G>A (p.Val203=)	rs776703291	0.00001
NM_000162.5(GCK):c.-450C>T
NM_000162.5(GCK):c.1020-8C>T
NM_000162.5(GCK):c.1233C>G (p.Ser411=)	rs755112715
NM_000162.5(GCK):c.369C>T (p.Phe123=)
NM_000162.5(GCK):c.46-11T>A
NM_000162.5(GCK):c.46-14C>A
NM_000162.5(GCK):c.468C>T (p.His156=)
NM_000162.5(GCK):c.765C>T (p.Thr255=)

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