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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERCC2
(A717G)
Single nucleotide variant
(missense variant)
not provided
+7 more
GPathogenic/Likely pathogenic
ERCC2
(P694S)
Single nucleotide variant
(missense variant)
Leukodystrophy
+2 more
GConflicting classifications of pathogenicity
ERCC2
(F568fs)
Deletion
(frameshift variant)
not provided
+7 more
GPathogenic/Likely pathogenic
ERCC2
(L461V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
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