ClinVar Miner

List of variants in gene SCNN1B reported as uncertain significance for Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000336.3(SCNN1B):c.1513C>T (p.Arg505Cys)

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