ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as uncertain significance for SUDDEN INFANT DEATH SYNDROME; Brugada syndrome

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000335.5(SCN5A):c.2989G>A (p.Ala997Thr) rs137854609 0.00008

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