Variants with conflicting interpretations "uncertain significance" from GeneDx and "likely benign" from Natera, Inc.

Minimum review status of the submission from GeneDx:		Collection method of the submission from GeneDx:
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_000498.3(CYP11B2):c.182A>T (p.Tyr61Phe)	rs147109119	0.00160
NM_015506.3(MMACHC):c.332G>A (p.Arg111Gln)	rs200300254	0.00123
NM_000128.4(F11):c.797G>A (p.Ser266Asn)	rs145168351	0.00081
NM_000094.4(COL7A1):c.3809C>T (p.Pro1270Leu)	rs145068043	0.00032
NM_000352.6(ABCC8):c.1958G>A (p.Arg653Gln)	rs146378237	0.00006
NM_000352.6(ABCC8):c.2235C>T (p.Ser745=)	rs200708414	0.00003
NM_000352.6(ABCC8):c.495G>A (p.Ser165=)	rs369136858	0.00003
NM_005629.4(SLC6A8):c.1285C>G (p.Leu429Val)	rs782551106	0.00003
NM_015506.3(MMACHC):c.800G>A (p.Arg267Gln)	rs765822392	0.00002

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