List of variants in gene CNTN2 reported as likely benign 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_005076.5(CNTN2):c.505C>T (p.Leu169Phe)	rs142502980	0.00224
NM_005076.5(CNTN2):c.223A>G (p.Met75Val)	rs144767577	0.00047
NM_005076.5(CNTN2):c.2577A>G (p.Ala859=)

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