ClinVar Miner

List of variants reported as not provided for SCN5A-related disorder by GenomeConnect, ClinGen

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000335.5(SCN5A):c.5827C>T (p.Arg1943Ter) rs794728940 0.00004
NM_000335.5(SCN5A):c.3985G>A (p.Ala1329Thr) rs199473224

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