ClinVar Miner

List of variants reported as uncertain significance for autosomal dominant nocturnal frontal lobe epilepsy by Division of Human Genetics, Children's Hospital of Philadelphia

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_000744.7(CHRNA4):c.274G>C (p.Glu92Gln)	rs146651027	0.00029
NM_000744.7(CHRNA4):c.1316A>C (p.Lys439Thr)	rs796052318	0.00009

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