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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNB2
(A427T)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GBenign
LMNB2
(R235Q)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+4 more
GBenign/Likely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(E48K)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
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