ClinVar Miner

List of variants in gene MYO7A reported as likely benign by ClinGen Hearing Loss Variant Curation Expert Panel,

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_000260.4(MYO7A):c.905G>A (p.Arg302His) rs41298135

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