ClinVar Miner

List of variants in gene SCN8A reported as uncertain significance for Intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.993-58A>G	rs74091614	0.03307
NM_001330260.2(SCN8A):c.1236_1251del (p.Met412fs)	rs1941768692

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