List of variants in gene combination LOC105371566, MYO15A reported as uncertain significance 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.-227G>A	rs185186294	0.00100
NM_016239.4(MYO15A):c.-223G>T	rs1027357950
NM_016239.4(MYO15A):c.-224C>T	rs189693278
NM_016239.4(MYO15A):c.-236C>A	rs890566879

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