"PreventionGenetics, part of Exact Sciences"[submitter] AND "PDIA3"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 714532	NM_005313.5(PDIA3):c.168-9C>T	PDIA3	Single nucleotide variant (intron variant)	PDIA3-related disorder +1 more	GBenign
Select item 1250388	NM_005313.5(PDIA3):c.365-5C>T	PDIA3	Single nucleotide variant (intron variant)	PDIA3-related disorder +1 more	GBenign
Select item 3046366	NM_005313.5(PDIA3):c.472+7A>G	PDIA3	Single nucleotide variant (intron variant)	PDIA3-related disorder	GLikely benign
Select item 3055506	NM_005313.5(PDIA3):c.603-5_603-4dup	PDIA3	Duplication (intron variant)	PDIA3-related disorder	GLikely benign
Select item 727555	NM_005313.5(PDIA3):c.858G>A (p.Val286=)	PDIA3	Single nucleotide variant (synonymous variant)	PDIA3-related disorder +1 more	GBenign
Select item 1257424	NM_005313.5(PDIA3):c.1224C>T (p.His408=)	PDIA3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3052887	NM_005313.5(PDIA3):c.1260C>T (p.Gly420=)	PDIA3	Single nucleotide variant (synonymous variant)	PDIA3-related disorder	GLikely benign
Select item 3060881	NM_005313.5(PDIA3):c.1458C>T (p.Asn486=)	PDIA3	Single nucleotide variant (synonymous variant)	PDIA3-related disorder	GBenign

ClinVar