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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANXA11, LOC126860977
Single nucleotide variant
(intron variant)
Inclusion body myopathy and brain white matter abnormalities
+1 more
GBenign
ANXA11, LOC126860977
Single nucleotide variant
(intron variant)
Inclusion body myopathy and brain white matter abnormalities
+1 more
GBenign