Variants with conflicting interpretations "benign" from Eurofins Ntd Llc (ga) and "uncertain significance" from Center for Genetic Medicine Research, Children's National Medical Center

Minimum review status of the submission from Eurofins Ntd Llc (ga):		Collection method of the submission from Eurofins Ntd Llc (ga):
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024301.5(FKRP):c.341C>G (p.Ala114Gly)	rs143793528	0.00910
NM_004369.4(COL6A3):c.4156G>A (p.Glu1386Lys)	rs146092501	0.00602

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