Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR An irish case of limb-girdle muscular dystrophy 2I with structural eye involvement. 26833294

2016

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations. 26363967

2015

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans. 26574668

2015

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Diagnostic clues and manifesting carriers in fukutin-related protein (FKRP) limb-girdle muscular dystrophy. 25560911

2015

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Clinical and muscle biopsy findings in Norwegian paediatric patients with limb girdle muscular dystrophy 2I. 24447024

2014

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Muscle and heart function restoration in a limb girdle muscular dystrophy 2I (LGMD2I) mouse model by systemic FKRP gene delivery. 25048216

2014

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Mouse models of fukutin-related protein mutations show a wide range of disease phenotypes. 23591631

2013

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2I. 23576288

2013

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Cortical heterotopia in LGMD2I. 22264518

2012

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Carrier testing for severe childhood recessive diseases by next-generation sequencing. 21228398

2011

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Frequency of the FKRP mutation c.826C>A in isolated hyperCKemia and in limb girdle muscular dystrophy type 2 in German patients. 19820980

2010

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Mutations alter secretion of fukutin-related protein. 19900540

2010

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes. 19835634

2009

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Fukutin-related protein localizes to the Golgi apparatus and mutations lead to mislocalization in muscle in vivo. 17554798

2007

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments. 18593008

2006

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. 16634037

2006

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation. 15833432

2005

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR A second LGMD locus, LGMD2I, was identified in chromosome region 19q13.3, and the causative mutation was identified as c.826C>A (L276I), a missense mutation in the FKRP gene. 15580560

2005

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cells. 15574464

2005

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. 15060126

2004

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Phenotypic spectrum associated with mutations in the fukutin-related protein gene. 12666124

2003

dbSNP: rs28937900
rs28937900
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
A 0.730 CausalMutation CLINVAR Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 11741828

2001