Variants with conflicting interpretations "uncertain significance" from Institute of Human Genetics, University of Goettingen and "pathogenic" from any submitter

Minimum review status of the submission from Institute of Human Genetics, University of Goettingen:		Collection method of the submission from Institute of Human Genetics, University of Goettingen:
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_004820.5(CYP7B1):c.1061G>A (p.Ser354Asn)	rs753708048	0.00001
NM_003119.4(SPG7):c.1967G>C (p.Arg656Pro)	rs373143136

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