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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC106694316, MPO
(R569W)
Single nucleotide variant
(missense variant)
Alzheimer disease type 1
+2 more
GPathogenic/Likely pathogenic
LOC106694316, MPO
(R460Q)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity