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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB27A
(M119V)
Single nucleotide variant
(missense variant)
Griscelli syndrome type 2
+1 more
GUncertain significance
RAB27A
Single nucleotide variant
(5 prime UTR variant)
Autoinflammatory syndrome
+1 more
GUncertain significance