C0342277[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 503699	NM_000162.5(GCK):c.1155del (p.Leu386fs)	GCK (L385fs +5 more)	Deletion (frameshift variant)	Permanent neonatal diabetes mellitus 1 +4 more	GPathogenic/Likely pathogenic
Select item 2441736	NM_000162.5(GCK):c.692A>T (p.Asn231Ile)	GCK (N230I +2 more)	Single nucleotide variant (missense variant)	Permanent neonatal diabetes mellitus 1 +3 more	GUncertain significance
Select item 16134	NM_000162.5(GCK):c.683C>T (p.Thr228Met)	GCK (T228M +2 more)	Single nucleotide variant (missense variant)	Monogenic diabetes	GPathogenic FDA Recognized database
Select item 1028584	NM_000162.5(GCK):c.415A>T (p.Met139Leu)	GCK (M139L +2 more)	Single nucleotide variant (missense variant)	Maturity onset diabetes mellitus in young +4 more	GUncertain significance
Select item 16138	NM_000162.5(GCK):c.391T>C (p.Ser131Pro)	GCK (S131P +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GLikely pathogenic
Select item 36206	NM_000162.5(GCK):c.208+11G>A	GCK	Single nucleotide variant (intron variant)	Maturity-onset diabetes of the young type 2 +6 more	GConflicting classifications of pathogenicity

ClinVar