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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POMGNT2
Single nucleotide variant
(synonymous variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+3 more
GBenign/Likely benign
POMGNT2
(R462W)
Single nucleotide variant
(missense variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+2 more
GBenign/Likely benign
POMGNT2
Single nucleotide variant
(synonymous variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+2 more
GConflicting classifications of pathogenicity
POMGNT2
(V122M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
POMGNT2
(R24Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
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