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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADA2
(R169Q +2 more)
Single nucleotide variant
(missense variant)
Sneddon syndrome
+4 more
GPathogenic/Likely pathogenic
ADA2
(G47V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic