List of variants in gene combination EYA4, TARID reported as uncertain significance for Dilated cardiomyopathy 1J; Autosomal dominant nonsyndromic hearing loss 10

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004100.5(EYA4):c.*2511G>A	rs560590444	0.00040
NM_004100.5(EYA4):c.*3226A>C	rs73546871	0.00035
NM_004100.5(EYA4):c.*1943C>T	rs150567885	0.00007
NM_004100.5(EYA4):c.*3267C>A	rs886061099	0.00006
NM_004100.5(EYA4):c.*732A>G	rs902919934	0.00004
NM_004100.5(EYA4):c.*2049T>C	rs752513150	0.00003
NM_004100.5(EYA4):c.*1551G>T	rs895041455	0.00001
NM_004100.5(EYA4):c.1822G>C (p.Glu608Gln)	rs1173508611	0.00001
NM_004100.5(EYA4):c.*1532G>A	rs776008831
NM_004100.5(EYA4):c.1358C>A (p.Thr453Asn)	rs1321644184

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