List of variants in gene CBL reported as likely pathogenic for Noonan syndrome

Minimum submission review status:		Collection method:
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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_005188.4(CBL):c.1096-4_1096-1del	rs397517077
NM_005188.4(CBL):c.1099C>A (p.Gln367Lys)	rs727504504
NM_005188.4(CBL):c.1228-2A>G	rs727504426

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