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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNB2
(G599D)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GConflicting classifications of pathogenicity
LMNB2
(D297E)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
GUncertain significance
LMNB2
(H191R)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(A94V)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GConflicting classifications of pathogenicity
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+2 more
GConflicting classifications of pathogenicity
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