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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATM
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic/Likely pathogenic
C11orf65, ATM
(R2598*)
Single nucleotide variant
(nonsense +1 more)
not provided
+4 more
GPathogenic
ATM, C11orf65
(R2993*)
Single nucleotide variant
(nonsense +1 more)
Familial cancer of breast
+4 more
GPathogenic/Likely pathogenic
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