Variants with conflicting interpretations "likely pathogenic" from Baylor Genetics and "uncertain significance" from PreventionGenetics, part of Exact Sciences

Minimum review status of the submission from Baylor Genetics:		Collection method of the submission from Baylor Genetics:
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_130837.3(OPA1):c.1311A>G (p.Ile437Met)	rs143319805	0.00056
NM_005912.3(MC4R):c.508A>G (p.Ile170Val)	rs121913560	0.00016
NM_000275.3(OCA2):c.2079G>A (p.Glu693=)	rs1374558186	0.00001

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