List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 31 by Genome-Nilou Lab

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.2256= (p.Gln752=)	rs6478078	0.99456
NM_015404.4(WHRN):c.1091= (p.His364=)	rs10817610	0.98173
NM_015404.4(WHRN):c.1353T>C (p.Gly451=)	rs4979387	0.76260
NM_015404.4(WHRN):c.1838T>C (p.Met613Thr)	rs942519	0.47944
NM_015404.4(WHRN):c.2348T>C (p.Val783Ala)	rs2274159	0.40624
NM_015404.4(WHRN):c.117G>A (p.Val39=)	rs2297815	0.33019
NM_015404.4(WHRN):c.964-21A>G	rs2274163	0.31128
NM_015404.4(WHRN):c.1627-12G>A	rs2274160	0.23283
NM_015404.4(WHRN):c.1318G>A (p.Ala440Thr)	rs4978584	0.19569
NM_015404.4(WHRN):c.1416+22A>T	rs4979386	0.19539
NM_015404.4(WHRN):c.2388C>A (p.Asn796Lys)	rs2274158	0.19185

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