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

Minimum review status of the submission from Institute of Human Genetics, University Hospital of Duesseldorf:		Collection method of the submission from Institute of Human Genetics, University Hospital of Duesseldorf:
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_015107.3(PHF8):c.1731-2A>G	rs1437750762	0.00001
NM_000161.3(GCH1):c.689T>C (p.Met230Thr)	rs2140038798
NM_006852.6(TLK2):c.890G>A (p.Gly297Asp)	rs1555639254

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