"GeneDx"[submitter] AND "PTH"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 303700	NM_000315.4(PTH):c.*319A>G	PTH	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 1178813	NM_000315.4(PTH):c.187_188del	PTH	Deletion (3 prime UTR variant)	not provided	GBenign
Select item 255817	NM_000315.4(PTH):c.247C>A (p.Arg83=)	PTH	Single nucleotide variant (synonymous variant)	Familial hypoparathyroidism +3 more	GBenign
Select item 379458	NM_000315.4(PTH):c.166C>T (p.Arg56Cys)	PTH (R56C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1289830	NM_000315.4(PTH):c.87-50G>A	PTH	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276241	NM_000315.4(PTH):c.-5-98G>A	PTH	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar