"OMIM"[submitter] AND "CSRP3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8780	NM_003476.5(CSRP3):c.206A>G (p.Lys69Arg)	CSRP3 (K69R)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 8777	NM_003476.5(CSRP3):c.172T>G (p.Cys58Gly)	CSRP3 (C58G)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 8779	NM_003476.5(CSRP3):c.160_164delinsAGGGG (p.Ser54_Glu55delinsArgGly)	CSRP3	Indel (missense variant +1 more)	Hypertrophic cardiomyopathy 12	GPathogenic
Select item 8781	NM_003476.5(CSRP3):c.136A>C (p.Ser46Arg)	CSRP3 (S46R)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy 12 +5 more	GUncertain significance
Select item 8778	NM_003476.5(CSRP3):c.131T>C (p.Leu44Pro)	CSRP3 (L44P)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 8776	NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg)	CSRP3 (W4R)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +9 more	GConflicting classifications of pathogenicity

ClinVar