Variants with conflicting interpretations "benign" from Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center and "likely benign" from any submitter

Minimum review status of the submission from Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center:		Collection method of the submission from Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-9G>A	rs12313763	0.08467
NM_002834.5(PTPN11):c.255C>T (p.His85=)	rs61736914	0.02271
NM_002755.4(MAP2K1):c.711G>A (p.Gly237=)	rs17586159	0.01226
NM_004333.6(BRAF):c.-19C>T	rs71645935	0.01115
NM_002834.5(PTPN11):c.525+12G>C	rs41304351	0.01035
NM_005633.4(SOS1):c.1964C>T (p.Pro655Leu)	rs56219475	0.00787
NM_005633.4(SOS1):c.1074+5G>C	rs145155424	0.00655

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