Variants with conflicting interpretations "other" from Eurofins Ntd Llc (ga) and "uncertain significance" from Labcorp Genetics (formerly Invitae), Labcorp

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000463.3(UGT1A1):c.1091C>T (p.Pro364Leu)	rs34946978	0.00053
NM_000463.3(UGT1A1):c.686C>A (p.Pro229Gln)	rs35350960
Single allele

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