"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 239629	NM_004100.5(EYA4):c.277+9G>A	EYA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1J +2 more	GBenign/Likely benign
Select item 44772	NM_004100.5(EYA4):c.783G>A (p.Thr261=)	EYA4	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 10 +4 more	GConflicting classifications of pathogenicity
Select item 239632	NM_004100.5(EYA4):c.987G>T (p.Met329Ile)	EYA4 (M329I +4 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 192118	NM_004100.5(EYA4):c.1035G>C (p.Arg345Ser)	EYA4 (R345S +4 more)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 10 +4 more	GConflicting classifications of pathogenicity
Select item 355447	NM_004100.5(EYA4):c.1338A>G (p.Leu446=)	EYA4, TARID	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 36031	NM_004100.5(EYA4):c.1845C>T (p.Asn615=)	EYA4, TARID	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 10 +4 more	GBenign/Likely benign

ClinVar