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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SGCB
(G315R)
Single nucleotide variant
(missense variant)
Limb-girdle muscular dystrophy, recessive
+4 more
GConflicting classifications of pathogenicity
SGCB
(S302G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SGCB
(D281N)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2E
+1 more
GUncertain significance
SGCB
(I166V)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
SGCB
(L64S)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2E
+2 more
GUncertain significance
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