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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHST8
(R77W)
Single nucleotide variant
(missense variant)
Peeling skin syndrome type A
+1 more
GConflicting classifications of pathogenicity
CHST8
(V186A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance