ClinVar Miner

List of variants in gene combination CHRNA4, LOC126863087 reported as uncertain significance for Autosomal dominant nocturnal frontal lobe epilepsy 1

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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_000744.7(CHRNA4):c.274G>C (p.Glu92Gln)	rs146651027	0.00029
NM_000744.7(CHRNA4):c.245T>C (p.Met82Thr)	rs2068719750

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