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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMOD3
(Q405E)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
+1 more
GUncertain significance
LMOD3
(I263T)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
+1 more
GConflicting classifications of pathogenicity
LMOD3, LOC126806710
(D56N)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
GUncertain significance
LMOD3, LOC126806710
(A43T)
Single nucleotide variant
(missense variant)
Nemaline myopathy 10
GUncertain significance
LMOD3, LOC126806710
(S8*)
Single nucleotide variant
(nonsense)
Nemaline myopathy 10
GLikely pathogenic
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