List of variants in gene MYO3A reported as likely benign for auditory system disorder

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_017433.5(MYO3A):c.1743G>A (p.Glu581=)	rs41279908	0.09706
NM_017433.5(MYO3A):c.-132A>G	rs7073224	0.08457
NM_017433.4(MYO3A):c.-215A>G	rs7073084	0.08165
NM_017433.5(MYO3A):c.624C>T (p.Asp208=)	rs35010955	0.07818
NM_017433.5(MYO3A):c.660C>T (p.Ala220=)	rs34067308	0.06790
NM_017433.5(MYO3A):c.2497G>T (p.Ala833Ser)	rs33947968	0.06112
NM_017433.5(MYO3A):c.*246C>T	rs12261671	0.02109
NM_017433.5(MYO3A):c.-189C>G	rs188597967	0.01399
NM_017433.5(MYO3A):c.4335A>G (p.Lys1445=)	rs34615182	0.01332
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile)	rs33968748	0.01220
NM_017433.5(MYO3A):c.3094G>A (p.Ala1032Thr)	rs34918608	0.00803
NM_017433.5(MYO3A):c.3589G>A (p.Glu1197Lys)	rs75801377	0.00400
NM_017433.5(MYO3A):c.4462A>G (p.Lys1488Glu)	rs34204285	0.00188
NM_017433.5(MYO3A):c.115T>C (p.Leu39=)	rs764861194	0.00001
NM_017433.5(MYO3A):c.905C>T (p.Thr302Met)	rs753270542	0.00001

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