ClinVar Miner

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

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His)	rs45629132
NM_000260.4(MYO7A):c.1817G>A (p.Arg606His)	rs782311929
NM_000260.4(MYO7A):c.2476G>A (p.Ala826Thr)	rs368341987

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