List of variants in gene MYO15A reported as likely pathogenic for Hearing impairment

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.2677C>T (p.Arg893Ter)	rs763075073	0.00001
NM_016239.4(MYO15A):c.4039A>T (p.Ile1347Phe)	rs375627187	0.00001
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs)	rs750130520
NM_016239.4(MYO15A):c.2873del (p.Pro958fs)	rs1217492313
NM_016239.4(MYO15A):c.4240G>A (p.Glu1414Lys)	rs1060499798
NM_016239.4(MYO15A):c.9467T>C (p.Leu3156Pro)	rs2046774616
NM_016239.4(MYO15A):c.9620G>T (p.Arg3207Leu)	rs199621031

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