List of variants in gene GCK reported as likely pathogenic for pregnancy disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.787T>C (p.Ser263Pro)	rs193922331	0.00001
NM_000162.5(GCK):c.1112G>T (p.Cys371Phe)	rs587780343
NM_000162.5(GCK):c.616A>C (p.Thr206Pro)	rs587780346

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