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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XRCC4
(W43R)
Single nucleotide variant
(missense variant)
Short stature, microcephaly, and endocrine dysfunction
+1 more
GPathogenic/Likely pathogenic
XRCC2
(R215*)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity