Related gene-specific medical variations for Gene (Select 79772) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124488	NM_024717.7(MCTP1):c.376C>G (p.Arg126Gly)	LOC129994224, MCTP1 (R126G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124487	NM_024717.7(MCTP1):c.322G>C (p.Glu108Gln)	LOC129994224, MCTP1 (E108Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124481	NM_024717.7(MCTP1):c.178C>T (p.Pro60Ser)	LOC129994225, MCTP1 (P60S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391819	NM_024717.7(MCTP1):c.316C>T (p.Pro106Ser)	LOC129994224, MCTP1 (P106S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261916	NM_024717.7(MCTP1):c.287A>C (p.Gln96Pro)	LOC129994224, MCTP1 (Q96P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 156978	Single allele	MCTP1	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided

ClinVar