"GeneDx"[submitter] AND "LOC126859796"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1296321	NM_004100.5(EYA4):c.1192-96T>C	EYA4, LOC126859796 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3370193	NM_004100.5(EYA4):c.1211C>A (p.Thr404Asn)	EYA4, LOC126859796 +1 more (T350N +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2430587	NM_004100.5(EYA4):c.1216G>A (p.Gly406Arg)	EYA4, LOC126859796 +1 more (G352R +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1712119	NM_004100.5(EYA4):c.1226T>G (p.Met409Arg)	EYA4, LOC126859796 +1 more (M355R +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GUncertain significance
Select item 1693092	NM_004100.5(EYA4):c.1261T>G (p.Leu421Val)	EYA4, LOC126859796 +1 more (L367V +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1J +1 more	GUncertain significance
Select item 1262043	NM_004100.5(EYA4):c.1281+21A>G	EYA4, LOC126859796 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1J +1 more	GBenign
Select item 1205373	NM_004100.5(EYA4):c.1281+23A>G	EYA4, LOC126859796 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

ClinVar