List of variants in gene combination C17orf107, CHRNE reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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.710G>T (p.Arg237Leu)	rs201434993	0.00010
NM_000080.4(CHRNE):c.37G>A (p.Gly13Arg)	rs372635387	0.00002
NM_000080.4(CHRNE):c.917+372C>T

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