List of variants in gene CNTN1 reported as not provided for hereditary skeletal muscle disorder

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_001843.4(CNTN1):c.643A>G (p.Ser215Gly)	rs138639141	0.00015
NM_001843.4(CNTN1):c.1006C>T (p.His336Tyr)	rs200591895	0.00012
NM_001843.4(CNTN1):c.1024G>A (p.Val342Met)	rs200139062	0.00012

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