List of variants in gene CHRNE reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000080.4(CHRNE):c.1115C>T (p.Ala372Val)	rs912512352	0.00006
NM_000080.4(CHRNE):c.1018C>T (p.Pro340Ser)	rs1019584942
NM_000080.4(CHRNE):c.1254dup (p.Glu419fs)	rs769945146
NM_000080.4(CHRNE):c.1353dup (p.Asn452fs)	rs773526895
NM_000080.4(CHRNE):c.1402G>C (p.Val468Leu)	rs139171143
NM_000080.4(CHRNE):c.1429del (p.Ala477fs)	rs1396286715

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