List of variants in gene combination CHRNE, LOC130060041 reported as benign for neuromuscular junction disease

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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.1033-6C>T	rs2075763	0.06582
NM_000080.4(CHRNE):c.1076C>T (p.Pro359Leu)	rs192195094	0.00240
NM_000080.4(CHRNE):c.1033-9del

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