List of variants reported as benign for autosomal recessive nonsyndromic hearing loss 29 by Illumina Laboratory Services, Illumina

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001146079.2(CLDN14):c.-264G>C	rs188733	0.34950
NM_001146079.2(CLDN14):c.-290A>G	rs219742	0.34026
NM_001146079.2(CLDN14):c.243C>T (p.Arg81=)	rs219779	0.25678
NM_001146079.2(CLDN14):c.687G>A (p.Thr229=)	rs219780	0.20318
NM_001146079.2(CLDN14):c.633C>T (p.Tyr211=)	rs61745291	0.01969
NM_001146079.2(CLDN14):c.300C>T (p.Ile100=)	rs113350364	0.00136

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