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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERCC6
(R666C)
Single nucleotide variant
(missense variant)
not specified
+12 more
GConflicting classifications of pathogenicity
ERCC6, PGBD3
(G446D)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign/Likely benign
ERCC6, PGBD3
(D386E)
Single nucleotide variant
(missense variant +1 more)
ERCC6-related condition
+5 more
GConflicting classifications of pathogenicity
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