List of variants reported as uncertain significance for hereditary continuous muscle fiber activity by Revvity Omics, Revvity

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000217.3(KCNA1):c.61G>A (p.Asp21Asn)	rs747465523	0.00002
NM_000217.3(KCNA1):c.16G>A (p.Gly6Arg)	rs754549386
NM_000217.3(KCNA1):c.457G>T (p.Val153Leu)
NM_000217.3(KCNA1):c.502G>A (p.Val168Ile)
NM_000217.3(KCNA1):c.608A>G (p.His203Arg)

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