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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMN, LOC130056553
Single nucleotide variant
(intron variant)
Imerslund-Grasbeck syndrome
+2 more
GBenign/Likely benign
AMN, CDC42BPB
+1 more
Single nucleotide variant
(splice acceptor variant)
Imerslund-Grasbeck syndrome type 2
+2 more
GPathogenic