U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 1 to 100 of 519

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNB2
(E279V)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(K381Q)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(G457S)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(G535S)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(A135V)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2, LOC130063066
(A18V)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(T612I)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(S553I)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(I522V)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(L25V)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(E442D)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(G91D)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(A596G)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(P542S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2, LOC130063065
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(L317F)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(S541R)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(E585D)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(S410L)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(S168N)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(G190S)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(S98L)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(N132I)
Indel
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2, LOC130063066
(R14G)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(T530M)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(S405F)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+2 more
GLikely benign
LMNB2
(A514T)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(R240H)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(A536T)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(R211C)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(E477K)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
CSNK1G2, PEAK3
+35 more
Duplication
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2, LOC130063066
(S5N)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(G429R)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2, MIR7108
Single nucleotide variant
(non-coding transcript variant +1 more)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(A94G)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(R239Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(R236Q)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(S159R)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(G190R)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(R272W)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(intron variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(T418P)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2, LOC130063065
(R87H)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(V565L)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Microsatellite
(intron variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(E482K)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
LMNB2
(G446D)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(S247R)
Single nucleotide variant
(missense variant)
LMNB2-related disorder
+2 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 9
+1 more
GLikely benign
LMNB2
(V529I)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(V577M)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
(S559R)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GBenign
LMNB2
(Q146R)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(R346Q)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 9
+1 more
GUncertain significance
LMNB2
(V582M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
LMNB2
(T454R)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
(V131I)
Single nucleotide variant
(missense variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GUncertain significance
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
LMNB2
Single nucleotide variant
(synonymous variant)
Lipodystrophy, partial, acquired, susceptibility to
+1 more
GLikely benign
Format
Items per page
Sort by
Choose Destination