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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERCC6L2
(W367R)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GUncertain significance
ERCC6L2
(R644*)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
ERCC6L2
Single nucleotide variant
(synonymous variant +1 more)
Pancytopenia-developmental delay syndrome
+1 more
GBenign/Likely benign
ERCC6L2
(Q1280P)
Single nucleotide variant
(missense variant +2 more)
not provided
+2 more
GLikely benign
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