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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERCC2
(R497C)
Single nucleotide variant
(missense variant)
Cerebrooculofacioskeletal syndrome 2
+1 more
GUncertain significance
ERCC2
(A202S +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ERCC2
(H124Y +1 more)
Single nucleotide variant
(missense variant)
Trichothiodystrophy 1, photosensitive
+4 more
GConflicting classifications of pathogenicity
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