Variants with conflicting interpretations "uncertain significance" from Pathway Genomics and "likely benign" from any submitter

Minimum review status of the submission from Pathway Genomics:		Collection method of the submission from Pathway Genomics:
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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.1062C>G (p.Phe354Leu)	rs59912467	0.00348
NM_000038.6(APC):c.1604C>T (p.Ser535Phe)	rs75870842	0.00071
NM_000038.6(APC):c.1240C>T (p.Arg414Cys)	rs137854567	0.00053
NM_000535.7(PMS2):c.857A>G (p.Asp286Gly)	rs116788608	0.00011
NM_000038.6(APC):c.6473C>G (p.Pro2158Arg)	rs587779804	0.00007
NM_000251.3(MSH2):c.2732T>G (p.Leu911Arg)	rs41295182	0.00007
NM_000038.6(APC):c.1685C>T (p.Thr562Met)	rs587783034	0.00002
NM_000455.5(STK11):c.465-4G>A	rs587780009
NM_007294.4(BRCA1):c.2998_3003del (p.Glu1000_Glu1001del)	rs80358333

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