List of variants in gene MYO15A reported as uncertain significance by Athena Diagnostics Inc

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.9181G>A (p.Glu3061Lys)	rs116833707	0.00089
NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu)	rs201689819	0.00036
NM_016239.4(MYO15A):c.10121G>A (p.Arg3374His)	rs201794696	0.00029
NM_016239.4(MYO15A):c.8347G>A (p.Val2783Met)	rs201214320	0.00023
NM_016239.4(MYO15A):c.9772G>A (p.Val3258Ile)	rs79745502	0.00014
NM_016239.4(MYO15A):c.4561G>C (p.Glu1521Gln)	rs769189017	0.00006
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter)	rs375290498	0.00005
NM_016239.4(MYO15A):c.9593T>C (p.Ile3198Thr)	rs369742063	0.00002
NM_016239.4(MYO15A):c.1277C>T (p.Ala426Val)	rs765664013	0.00001
NM_016239.4(MYO15A):c.3080C>T (p.Thr1027Ile)	rs1256708810
NM_016239.4(MYO15A):c.3259G>A (p.Ala1087Thr)
NM_016239.4(MYO15A):c.9985G>A (p.Val3329Met)	rs1597820494

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