Variants in gene CBL with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_005188.4(CBL):c.2345C>T (p.Pro782Leu)	rs2229073	0.00281
NM_005188.4(CBL):c.2363G>A (p.Arg788Gln)	rs150811339	0.00036
NM_005188.4(CBL):c.-5A>G	rs552214111	0.00013
NM_005188.4(CBL):c.2060C>T (p.Pro687Leu)	rs146705974	0.00012
NM_005188.4(CBL):c.2360G>A (p.Arg787His)	rs200220863	0.00011
NM_005188.4(CBL):c.195+3G>A	rs762062705	0.00004

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