List of variants reported as uncertain significance for Dilated cardiomyopathy 1J; Autosomal dominant nonsyndromic hearing loss 10 by Fulgent Genetics, Fulgent Genetics

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Total variants: 23

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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.148A>T (p.Ser50Cys)	rs932450184	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.1067G>A (p.Arg356Gln)	rs762144530	0.00003
NM_004100.5(EYA4):c.458C>G (p.Ser153Cys)	rs1554261941	0.00003
NM_004100.5(EYA4):c.860C>T (p.Ala287Val)	rs374522988	0.00003
NM_004100.5(EYA4):c.233C>G (p.Thr78Arg)	rs201644472	0.00002
NM_004100.5(EYA4):c.*1551G>T	rs895041455	0.00001
NM_004100.5(EYA4):c.1085C>T (p.Pro362Leu)	rs1168354526	0.00001
NM_004100.5(EYA4):c.1822G>C (p.Glu608Gln)	rs1173508611	0.00001
NM_004100.5(EYA4):c.213A>C (p.Glu71Asp)	rs200042576	0.00001
NM_004100.5(EYA4):c.529G>A (p.Val177Ile)	rs776409783	0.00001
NM_004100.5(EYA4):c.83+5A>G	rs1060502995	0.00001
NM_004100.5(EYA4):c.*1532G>A	rs776008831
NM_004100.5(EYA4):c.1358C>A (p.Thr453Asn)	rs1321644184
NM_004100.5(EYA4):c.32C>T (p.Ser11Leu)	rs1394230343
NM_004100.5(EYA4):c.686C>T (p.Pro229Leu)	rs769220102
NM_004100.5(EYA4):c.824C>T (p.Ala275Val)	rs748654006
NM_004100.5(EYA4):c.978C>G (p.Phe326Leu)	rs773095472

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