"PDLIM3-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 227013	NM_014476.6(PDLIM3):c.993C>A (p.Gly331=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	PDLIM3-related disorder +4 more	GBenign/Likely benign
Select item 201947	NM_014476.6(PDLIM3):c.696C>T (p.Asp232=)	PDLIM3	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 378350	NM_014476.6(PDLIM3):c.440G>A (p.Arg147His)	PDLIM3 (R147H)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 2630799	NM_014476.6(PDLIM3):c.331-411C>A	LOC126807246, PDLIM3 (A158E)	Single nucleotide variant (missense variant +1 more)	PDLIM3-related disorder	GUncertain significance
Select item 3052200	NM_014476.6(PDLIM3):c.331-497T>A	LOC126807246, PDLIM3	Single nucleotide variant (synonymous variant +1 more)	PDLIM3-related disorder	GLikely benign
Select item 1121320	NM_014476.6(PDLIM3):c.330+7G>A	PDLIM3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy +2 more	GLikely benign

ClinVar