"Revvity Omics, Revvity"[submitter] AND "GCM2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717588	NM_004752.4(GCM2):c.1395C>T (p.His465=)	GCM2	Single nucleotide variant (synonymous variant)	Familial hypoparathyroidism +1 more	GConflicting classifications of pathogenicity
Select item 1324460	NM_004752.4(GCM2):c.1109C>T (p.Thr370Met)	GCM2 (T370M)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2432091	NM_004752.4(GCM2):c.442G>A (p.Ala148Thr)	GCM2 (A148T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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