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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LBR
(R583*)
Single nucleotide variant
(nonsense)
Pelger-Huët anomaly
+6 more
GConflicting classifications of pathogenicity
LBR
(N547D)
Single nucleotide variant
(missense variant)
Pelger-Huët anomaly
+1 more
GPathogenic/Likely pathogenic
LBR
Single nucleotide variant
(intron variant)
Pelger-Huët anomaly
GUncertain significance
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