List of variants in gene combination CHRNB1, LOC130060147 reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000747.3(CHRNB1):c.6C>T (p.Thr2=)	rs755368307	0.00012
NM_000747.3(CHRNB1):c.39G>C (p.Leu13=)	rs770359368	0.00001
NM_000747.3(CHRNB1):c.51C>T (p.Leu17=)	rs1351230064	0.00001
NM_000747.3(CHRNB1):c.21G>C (p.Leu7=)
NM_000747.3(CHRNB1):c.9A>G (p.Pro3=)	rs1481997291

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