ClinVar Miner

List of variants reported as not provided for autosomal dominant nocturnal frontal lobe epilepsy by GenomeConnect - Invitae Patient Insights Network

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000748.3(CHRNB2):c.1046T>C (p.Met349Thr)	rs141735618	0.00010
NM_020822.3(KCNT1):c.32G>A (p.Gly11Glu)	rs1003586835	0.00006

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