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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAT4
(D4391V +2 more)
Single nucleotide variant
(missense variant)
Van Maldergem syndrome 2
GUncertain significance
NEB
(D3747A +1 more)
Single nucleotide variant
(missense variant)
Nemaline myopathy 2
GLikely pathogenic
KLHL40
(G469S)
Single nucleotide variant
(missense variant)
Nemaline myopathy 8
GConflicting classifications of pathogenicity
CREBBP
(R1867Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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