List of variants reported as likely benign for autosomal dominant nonsyndromic hearing loss 10 by Illumina Laboratory Services, Illumina

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_004100.5(EYA4):c.*2044A>G	rs59167148	0.00365
NM_004100.5(EYA4):c.783G>A (p.Thr261=)	rs17854076	0.00136
NM_004100.5(EYA4):c.*2588C>T	rs140401218	0.00078
NM_004100.5(EYA4):c.866C>T (p.Thr289Met)	rs41286200	0.00067
NM_004100.5(EYA4):c.*1905T>A	rs542036379	0.00060
NM_004100.5(EYA4):c.1035G>C (p.Arg345Ser)	rs140170914	0.00045
NM_004100.5(EYA4):c.*1350G>A	rs553570769	0.00018
NM_004100.5(EYA4):c.*2188T>A	rs376366555	0.00011
NM_004100.5(EYA4):c.*2359C>T	rs547907467	0.00004
NM_004100.5(EYA4):c.*1820A>T	rs184735364	0.00001
NM_004100.5(EYA4):c.899C>A (p.Ala300Asp)	rs757252384

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