Variants with conflicting interpretations "likely pathogenic" from Baylor Genetics and "pathogenic" 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1217C>T (p.Pro406Leu)	rs104894313	0.00375
NM_000372.5(TYR):c.1037-7T>A	rs61754381	0.00051
NM_000275.3(OCA2):c.2207C>T (p.Ser736Leu)	rs780296175	0.00003
NM_000287.4(PEX6):c.1287del (p.Trp430fs)	rs1258472160	0.00001
NM_000287.4(PEX6):c.1801C>T (p.Arg601Trp)	rs61753225	0.00001
NM_000275.3(OCA2):c.2177_2181del (p.Val726fs)	rs771620099
NM_000540.3(RYR1):c.12083C>T (p.Ser4028Leu)	rs794728696

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