List of variants reported as benign for autosomal recessive nonsyndromic hearing loss 37 by Illumina Laboratory Services, Illumina

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.*4114T>A	rs7766661	0.72931
NM_004999.4(MYO6):c.*3835C>T	rs7742137	0.51984
NM_004999.4(MYO6):c.*2027T>C	rs6914716	0.39546
NM_004999.4(MYO6):c.*3940T>C	rs11964034	0.33693
NM_004999.4(MYO6):c.*350T>C	rs699186	0.33478
NM_004999.4(MYO6):c.*12C>T	rs12606	0.22544
NM_004999.4(MYO6):c.*3447A>C	rs1341567	0.19296
NM_004999.4(MYO6):c.553+11T>C	rs12210963	0.13246
NM_004999.4(MYO6):c.*459A>G	rs1045758	0.13207
NM_004999.4(MYO6):c.*1703C>T	rs9360957	0.03977
NM_004999.4(MYO6):c.*3296G>T	rs7741414
NM_004999.4(MYO6):c.*4283A>G	rs7746476

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