Variants with conflicting interpretations "likely benign" from Spanish ATM Cancer Susceptibility Variant Interpretation Working Group and "benign" from any submitter

Minimum review status of the submission from Spanish ATM Cancer Susceptibility Variant Interpretation Working Group:		Collection method of the submission from Spanish ATM Cancer Susceptibility Variant Interpretation Working Group:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.162T>C (p.Tyr54=)	rs3218690	0.00200
NM_000051.4(ATM):c.609C>T (p.Asp203=)	rs144709948	0.00166
NM_000051.4(ATM):c.998C>T (p.Ser333Phe)	rs28904919	0.00133
NM_000051.4(ATM):c.1380G>C (p.Thr460=)	rs145333518

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