List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 21 by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.5171G>A (p.Ser1724Asn)	rs526433	0.99235
NM_005422.4(TECTA):c.1485A>G (p.Ala495=)	rs536069	0.76077
NM_005422.4(TECTA):c.2805T>C (p.Tyr935=)	rs586473	0.73877
NM_005422.4(TECTA):c.1111A>G (p.Arg371Gly)	rs612969	0.48670
NM_005422.4(TECTA):c.4098G>A (p.Thr1366=)	rs12275038	0.28426
NM_005422.4(TECTA):c.4105+13C>T	rs7130952	0.26144
NM_005422.4(TECTA):c.2256C>T (p.Ile752=)	rs10502247	0.25910
NM_005422.4(TECTA):c.5634C>T (p.Ser1878=)	rs2155369	0.10906

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