ClinVar Miner

List of variants in gene CHRNA2 reported as likely pathogenic for not provided

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000742.4(CHRNA2):c.1463C>T (p.Ser488Leu)	rs866092045	0.00001
NM_000742.4(CHRNA2):c.1293dup (p.Ser432fs)	rs751842443

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