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: 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.19G>A (p.Gly7Arg)	rs372509310	0.00043
NM_000260.4(MYO7A):c.2476G>A (p.Ala826Thr)	rs368341987	0.00042
NM_000260.4(MYO7A):c.2527G>A (p.Val843Met)	rs140559111	0.00024
NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn)	rs373147966	0.00023
NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln)	rs782396605	0.00009
NM_000260.4(MYO7A):c.3491G>A (p.Arg1164Gln)	rs782350886	0.00001
NM_000260.4(MYO7A):c.3827C>T (p.Ser1276Leu)	rs369458838	0.00001
NM_000260.4(MYO7A):c.1817G>A (p.Arg606His)	rs782311929
NM_000260.4(MYO7A):c.983T>C (p.Leu328Pro)	rs1281366817

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