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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMOD3, LOC126806710
(R83C)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
+1 more
GConflicting classifications of pathogenicity
LMOD3, LOC126806710
(V72I)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
GUncertain significance