Variants with conflicting interpretations "likely benign" from Giacomini Lab, University of California, San Francisco and "uncertain significance" from Labcorp Genetics (formerly Invitae), Labcorp

Minimum review status of the submission from Giacomini Lab, University of California, San Francisco:		Collection method of the submission from Giacomini Lab, University of California, San Francisco:
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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.115T>G (p.Ser39Ala)	rs544332057	0.00016
NM_003060.4(SLC22A5):c.1521G>C (p.Leu507Phe)	rs778716973	0.00002
NM_003060.4(SLC22A5):c.1621A>T (p.Met541Leu)	rs758158685	0.00001
NM_003060.4(SLC22A5):c.197C>T (p.Thr66Ile)	rs1169005119	0.00001
NM_003060.4(SLC22A5):c.575A>G (p.Asn192Ser)
NM_003060.4(SLC22A5):c.685A>C (p.Ile229Leu)

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