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

Minimum submission review status:		Collection method:
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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: 10

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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.1849T>C (p.Ser617Pro)	rs782063761
NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln)	rs782396605
NM_000260.4(MYO7A):c.2476G>A (p.Ala826Thr)	rs368341987
NM_000260.4(MYO7A):c.2527G>A (p.Val843Met)	rs140559111
NM_000260.4(MYO7A):c.3491G>A (p.Arg1164Gln)	rs782350886
NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn)	rs373147966
NM_000260.4(MYO7A):c.3827C>T (p.Ser1276Leu)	rs369458838
NM_000260.4(MYO7A):c.4115T>G (p.Val1372Gly)	rs869312181

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