List of variants in gene CBL reported as likely benign for Noonan-like syndrome

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005188.4(CBL):c.*1038del	rs555529036	0.00550
NM_005188.4(CBL):c.1360A>G (p.Asn454Asp)	rs371850672	0.00004
NM_005188.4(CBL):c.*3241dup	rs79093187
NM_005188.4(CBL):c.*5986del	rs541615597
NM_005188.4(CBL):c.*8288GTTA[1]	rs563997189
NM_005188.4(CBL):c.1228-10dup	rs397517078

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