Variants with conflicting interpretations "likely pathogenic" from Mayo Clinic Laboratories, Mayo Clinic and "risk factor" from any submitter

Minimum review status of the submission from Mayo Clinic Laboratories, Mayo Clinic:		Collection method of the submission from Mayo Clinic Laboratories, Mayo Clinic:
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_007194.4(CHEK2):c.470T>C (p.Ile157Thr)	rs17879961	0.00434
NM_001354604.2(MITF):c.1273G>A (p.Glu425Lys)	rs149617956	0.00160

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