List of variants in gene combination EYA4, TARID reported as benign for cardiomyopathy

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004100.5(EYA4):c.*1264T>A	rs9483585	0.99999
NM_004100.5(EYA4):c.*1434A>G	rs9483586	0.79868
NM_004100.5(EYA4):c.*23C>T	rs3734279	0.35809
NM_004100.5(EYA4):c.*2108A>G	rs17053541	0.24433
NM_004100.5(EYA4):c.*2184A>T	rs17053542	0.20492
NM_004100.5(EYA4):c.*726C>A	rs55805978	0.20466
NM_004100.5(EYA4):c.*1867C>T	rs17053540	0.15248
NM_004100.5(EYA4):c.*1658C>T	rs73546865	0.04226
NM_004100.5(EYA4):c.1845C>T (p.Asn615=)	rs142721902	0.00854
NM_004100.5(EYA4):c.1329G>A (p.Gly443=)	rs141300030	0.00067
NM_004100.5(EYA4):c.1617-13C>G	rs756045097	0.00018
NM_004100.5(EYA4):c.1501+19A>G	rs200678450	0.00015
NM_004100.5(EYA4):c.1418G>T (p.Gly473Val)	rs146977269	0.00014

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