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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL40
(C428fs)
Deletion
(frameshift variant)
Nemaline myopathy 8
GPathogenic
KLHL40
(T506P)
Single nucleotide variant
(missense variant)
Nemaline myopathy 8
GPathogenic
KLHL40
(E528K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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