Variants with conflicting interpretations "benign" from Spanish ATM Cancer Susceptibility Variant Interpretation Working Group and "likely benign" from True Health Diagnostics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.5558A>T (p.Asp1853Val)	rs1801673	0.00441
NM_000051.4(ATM):c.2362A>C (p.Ser788Arg)	rs641252	0.00265
NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	rs1800059	0.00169

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