ClinVar Miner

List of variants in gene KCNT1 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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_020822.3(KCNT1):c.1407C>G (p.His469Gln)	rs537722828	0.00003
NM_020822.3(KCNT1):c.3072C>T (p.Arg1024=)	rs141695705	0.00003

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