List of variants in gene MYO15A reported as likely benign for auditory system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7503G>A (p.Thr2501=)	rs16960961	0.02872
NM_016239.4(MYO15A):c.4533C>T (p.Ala1511=)	rs114328138	0.01906
NM_016239.4(MYO15A):c.3413A>G (p.Gln1138Arg)	rs76468019	0.01903
NM_016239.4(MYO15A):c.9708G>A (p.Val3236=)	rs115393178	0.01622
NM_016239.4(MYO15A):c.1791G>A (p.Ala597=)	rs114552047	0.01041
NM_016239.4(MYO15A):c.6796G>A (p.Val2266Met)	rs114274755	0.00791
NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser)	rs76707172	0.00765
NM_016239.4(MYO15A):c.2028C>A (p.Pro676=)	rs577023485	0.00762
NM_016239.4(MYO15A):c.9478C>T (p.Leu3160Phe)	rs140029076	0.00658
NM_016239.4(MYO15A):c.3026C>A (p.Pro1009His)	rs117612144	0.00347
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp)	rs145292219	0.00326
NM_016239.4(MYO15A):c.7655-7C>G	rs191171943	0.00211
NM_016239.4(MYO15A):c.10443G>A (p.Ala3481=)	rs190486507	0.00208
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp)	rs147458358	0.00177
NM_016239.4(MYO15A):c.1111C>A (p.Pro371Thr)	rs200382813	0.00153
NM_016239.4(MYO15A):c.10573A>G (p.Ser3525Gly)	rs182332665	0.00151
NM_016239.4(MYO15A):c.7908C>T (p.Ala2636=)	rs201535856	0.00118
NM_016239.4(MYO15A):c.1582G>A (p.Gly528Ser)	rs199695398	0.00111
NM_016239.4(MYO15A):c.3203G>T (p.Cys1068Phe)	rs189061214	0.00047
NM_016239.4(MYO15A):c.7069G>A (p.Gly2357Ser)	rs201540919	0.00034
NM_016239.4(MYO15A):c.9998G>A (p.Arg3333Gln)	rs200605472	0.00027
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter)	rs375290498	0.00005
NM_016239.4(MYO15A):c.*628C>G	rs55973639

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