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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AVP
(C116G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
AVP
(S87Y)
Single nucleotide variant
(missense variant)
not provided
GPathogenic/Likely pathogenic
AVP
(A19T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
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