List of variants reported as uncertain significance for nemaline myopathy 10 by Revvity Omics, Revvity

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_198271.5(LMOD3):c.247C>T (p.Arg83Cys)	rs200367429	0.00080
NM_198271.5(LMOD3):c.332G>A (p.Arg111His)	rs370401036	0.00004
NM_198271.5(LMOD3):c.1368C>G (p.Asn456Lys)
NM_198271.5(LMOD3):c.214G>A (p.Val72Ile)

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