ClinVar Miner

List of variants studied for Congenital myotonia, autosomal recessive form by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000083.3(CLCN1):c.501C>G (p.Phe167Leu) rs149729531 0.00075
NM_000083.3(CLCN1):c.1453A>G (p.Met485Val) rs146457619 0.00039
NM_000083.3(CLCN1):c.313C>T (p.Arg105Cys) rs201509501 0.00014
NM_000083.3(CLCN1):c.1649C>T (p.Thr550Met) rs762754992 0.00002
NM_000083.3(CLCN1):c.1444G>A (p.Gly482Arg) rs746125212 0.00001
NM_000083.3(CLCN1):c.502C>G (p.Pro168Ala)

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