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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POMK
(R15Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
POMK
(H59R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
POMK
(F268fs)
Deletion
(frameshift variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
+2 more
GConflicting classifications of pathogenicity
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