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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMN
(V442I)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 1
+3 more
GUncertain significance
BAG5, MIR380
+98 more
Copy number gain
not provided
GPathogenic