Variants with conflicting interpretations "pathogenic" from University Children's Hospital, University of Zurich and "uncertain significance" from any submitter

Minimum review status of the submission from University Children's Hospital, University of Zurich:		Collection method of the submission from University Children's Hospital, University of Zurich:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1004G>A (p.Arg335His)	rs543016186	0.00004
NM_005957.5(MTHFR):c.1088G>A (p.Arg363His)	rs786204023	0.00001
NM_005957.5(MTHFR):c.416C>T (p.Thr139Met)	rs1057519360	0.00001
NM_005957.5(MTHFR):c.767T>A (p.Ile256Asn)	rs373398993	0.00001
NM_005957.5(MTHFR):c.-13-28_-13-27del	rs1553188112
NM_005957.5(MTHFR):c.1060C>T (p.His354Tyr)	rs786204022
NM_005957.5(MTHFR):c.1606G>T (p.Val536Phe)	rs786204028
NM_005957.5(MTHFR):c.1793T>C (p.Leu598Pro)	rs786204034
NM_005957.5(MTHFR):c.643_645del (p.Lys215del)	rs746353274
NM_005957.5(MTHFR):c.760C>T (p.Pro254Ser)	rs786204017

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