Variants with conflicting interpretations "likely benign" from Genome Diagnostics Laboratory, Amsterdam University Medical Center and "likely benign" from any submitter

Minimum review status of the submission from Genome Diagnostics Laboratory, Amsterdam University Medical Center:		Collection method of the submission from Genome Diagnostics Laboratory, Amsterdam University Medical 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_000548.5(TSC2):c.5359G>A (p.Gly1787Ser)	rs45517419	0.00264
NM_000548.5(TSC2):c.3889G>A (p.Ala1297Thr)	rs45517319	0.00219
NM_000548.5(TSC2):c.5383C>T (p.Arg1795Cys)	rs45517423	0.00156
NM_000548.5(TSC2):c.1318G>A (p.Gly440Ser)	rs45484298	0.00111
NM_000548.5(TSC2):c.2476C>A (p.Leu826Met)	rs45517238	0.00073
NM_015046.7(SETX):c.4273A>G (p.Lys1425Glu)	rs534886444	0.00020
NM_000548.5(TSC2):c.4524CTT[1] (p.Phe1510del)	rs137854239

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