Variants in gene combination ATM, C11orf65 with conflicting interpretations reported as "risk factor and "pathogenic"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006

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