ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as uncertain significance by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001165963.4(SCN1A):c.5351T>A (p.Val1784Asp) rs1057518671

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