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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATM, C11orf65
(G1980R)
Single nucleotide variant
(missense variant +1 more)
Ataxia-telangiectasia syndrome
+2 more
GUncertain significance
C11orf65, ATM
Duplication
(intron variant)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
ATM, C11orf65
(H2981N)
Single nucleotide variant
(missense variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
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