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Items: 6

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr1:156104702
GRCh38:
Chr1:156134911
LMNADilated cardiomyopathy 1A, Benign scapuloperoneal muscular dystrophy with cardiomyopathy, Muscular dystrophy,
not provided
Pathogenic
(Dec 1, 2015)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr1:156084836
GRCh38:
Chr1:156115045
LMNAnot specified, not providedConflicting interpretations of pathogenicity
(Jan 10, 2017)
criteria provided, conflicting interpretations
3.
GRCh37:
Chr1:156104737-156104739
GRCh38:
Chr1:156134946-156134948
LMNAPrimary dilated cardiomyopathy, not providedPathogenic/Likely pathogenic
(May 9, 2017)
criteria provided, multiple submitters, no conflicts
4.
GRCh37:
Chr1:156104701
GRCh38:
Chr1:156134910
LMNAnot specifiedUncertain significance
(Aug 21, 2014)
criteria provided, single submitter
5.
GRCh37:
Chr1:156100449
GRCh38:
Chr1:156130658
LMNABenign scapuloperoneal muscular dystrophy with cardiomyopathy, not providedPathogenic
(Aug 9, 2003)
no assertion criteria provided
6.
GRCh37:
Chr1:156100449
GRCh38:
Chr1:156130658
LMNAFamilial partial lipodystrophy 2, Hutchinson-Gilford progeria syndrome, childhood-onset, Charcot-Marie-Tooth disease,
not provided
Pathogenic
(Apr 30, 2015)
no assertion criteria provided
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