List of variants in gene CHRNE reported as likely pathogenic by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000080.4(CHRNE):c.1434C>A (p.Tyr478Ter)	rs763943642	0.00002
NM_000080.4(CHRNE):c.1220-1G>C	rs373710822
NM_000080.4(CHRNE):c.1244_1257del (p.Ala415fs)	rs1555546224

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