List of variants in gene combination CBL, FRA11B, LOC130006894 reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005188.3(CBL):c.-126_-125insTGG	rs878976124
NM_005188.3(CBL):c.-126_-125insTGGCGG	rs758396206
NM_005188.3(CBL):c.-126_-125insTGGCGGCGGCGGCGGCGG	rs758396206
NM_005188.3(CBL):c.-127_-125GGC[12]	rs57028199
NM_005188.3(CBL):c.-127_-125GGC[13]	rs57028199
NM_005188.3(CBL):c.-127_-125GGC[14]	rs57028199
NM_005188.3(CBL):c.-127_-125GGC[15]	rs57028199
NM_005188.3(CBL):c.-127_-125GGC[8]	rs57028199
NM_005188.4(CBL):c.-125_-116delinsT	rs886047763

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