List of variants in gene combination EYA4, TARID reported as likely benign for 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)
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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004100.5(EYA4):c.*2799C>A	rs143596676	0.00882
NM_004100.5(EYA4):c.*2918G>A	rs75986250	0.00369
NM_004100.5(EYA4):c.*2044A>G	rs59167148	0.00365
NM_004100.5(EYA4):c.*2588C>T	rs140401218	0.00078
NM_004100.5(EYA4):c.*1905T>A	rs542036379	0.00060
NM_004100.5(EYA4):c.*1350G>A	rs553570769	0.00018
NM_004100.5(EYA4):c.1617-13C>G	rs756045097	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.1494C>T (p.Asn498=)	rs748934740	0.00001
NM_004100.5(EYA4):c.1840-16T>G	rs1039495587	0.00001

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