Variants with conflicting interpretations "likely pathogenic" from Eurofins Ntd Llc (ga) and "pathogenic" from CFTR-France

Minimum review status of the submission from Eurofins Ntd Llc (ga):		Collection method of the submission from Eurofins Ntd Llc (ga):
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_000492.4(CFTR):c.2856G>C (p.Met952Ile)	rs151048781	0.00006
NM_000492.4(CFTR):c.3095A>G (p.Tyr1032Cys)	rs144055758	0.00002

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