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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATM
(L1046P)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GLikely pathogenic
ATM
(L1322P)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia syndrome
+1 more
GConflicting classifications of pathogenicity