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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYNE2
(E5176V)
Single nucleotide variant
(missense variant)
Emery-Dreifuss muscular dystrophy 5, autosomal dominant
GUncertain significance
SYNE2
(R6379C +1 more)
Single nucleotide variant
(missense variant)
Emery-Dreifuss muscular dystrophy 5, autosomal dominant
+3 more
GConflicting classifications of pathogenicity
SYNE2
(R6657Q +3 more)
Single nucleotide variant
(missense variant)
Emery-Dreifuss muscular dystrophy 5, autosomal dominant
GUncertain significance
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