ClinVar Miner

List of variants in gene MYO3A reported as uncertain significance for Nonsyndromic Hearing Loss, Recessive

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_017433.4(MYO3A):c.-312G>A rs184554148 0.00035
NM_017433.5(MYO3A):c.2089T>G (p.Leu697Val) rs753357658 0.00003
NM_017433.4(MYO3A):c.-302G>C rs886046915
NM_017433.5(MYO3A):c.*399del rs558895234
NM_017433.5(MYO3A):c.*399dup rs558895234
NM_017433.5(MYO3A):c.-104-14del rs886046916
NM_017433.5(MYO3A):c.1053+11_1053+12inv
NM_017433.5(MYO3A):c.1286_1288del (p.Ile429_Ser430delinsThr) rs886046920

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