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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B3GALNT2
(C359Y)
Single nucleotide variant
(missense variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
GUncertain significance
B3GALNT2
(L289F)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
B3GALNT2
Single nucleotide variant
(splice acceptor variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
GPathogenic
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