U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POMGNT2
(P469L)
Single nucleotide variant
(missense variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+1 more
GUncertain significance
POMGNT2
(R407W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
POMGNT2
(K212R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
POMGNT2
(G200S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
POMGNT2
(G184S)
Single nucleotide variant
(missense variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+2 more
GUncertain significance
Format
Sort by
Choose Destination