List of variants in gene MYH14 reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss 4A

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.4297G>A (p.Glu1433Lys)	rs771755654	0.00006
NM_001145809.2(MYH14):c.2971G>A (p.Glu991Lys)	rs367588704	0.00001
NM_001145809.2(MYH14):c.571G>A (p.Asp191Asn)
NM_001145809.2(MYH14):c.571G>C (p.Asp191His)
NM_001145809.2(MYH14):c.587G>T (p.Cys196Phe)
NM_001145809.2(MYH14):c.693+1G>A

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