List of variants in gene EYA4 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004100.5(EYA4):c.829G>A (p.Gly277Ser)	rs9493627	0.37885
NM_004100.5(EYA4):c.-76C>T	rs78081370	0.04026
NM_004100.5(EYA4):c.804+17T>C	rs57845656	0.01673
NM_004100.5(EYA4):c.905G>A (p.Gly302Asp)	rs75133151	0.00860
NM_004100.5(EYA4):c.111T>C (p.Ser37=)	rs35863035	0.00620
NM_004100.5(EYA4):c.103C>T (p.Leu35=)	rs35562371	0.00597
NM_004100.5(EYA4):c.804+16G>T	rs13362743	0.00276
NM_004100.5(EYA4):c.783G>A (p.Thr261=)	rs17854076	0.00136
NM_004100.5(EYA4):c.277+9G>A	rs145320803	0.00072
NM_004100.5(EYA4):c.970+16C>G	rs201985955	0.00033
NM_004100.5(EYA4):c.873A>T (p.Gly291=)	rs761206775	0.00003
NM_004100.5(EYA4):c.580+14_580+16del	rs139659489
NM_004100.5(EYA4):c.725-9del	rs776867589
NM_004100.5(EYA4):c.867G>A (p.Thr289=)	rs763899252
NM_004100.5(EYA4):c.925A>G (p.Thr309Ala)	rs556335059

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