Gene: LAMA2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913570
rs121913570
LAMA2
0.800 GeneticVariation UNIPROT Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. 27234031

2017
dbSNP: rs121913570
rs121913570
LAMA2
0.800 GeneticVariation UNIPROT Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients. 24611677

2015
dbSNP: rs121913570
rs121913570
LAMA2
0.800 GeneticVariation UNIPROT Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 12552556

2003
dbSNP: rs121913570
rs121913570
LAMA2
0.800 GeneticVariation UNIPROT Consensus statement on standard of care for congenital muscular dystrophies. 21078917

2010
dbSNP: rs121913570
rs121913570
LAMA2
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913570
rs121913570
LAMA2
0.800 GeneticVariation UNIPROT Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study. 11591858

2001
dbSNP: rs1018100729
rs1018100729
LAMA2
T 0.700 GeneticVariation CLINVAR LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effect. 16216942

2005
dbSNP: rs1018100729
rs1018100729
LAMA2
T 0.700 GeneticVariation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs1055407857
rs1055407857
LAMA2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064797040
rs1064797040
LAMA2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064797327
rs1064797327
LAMA2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691660
rs1131691660
LAMA2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691660
rs1131691660
LAMA2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs117422805
rs117422805
LAMA2
0.700 GeneticVariation UNIPROT

dbSNP: rs1180309541
rs1180309541
LAMA2
T 0.700 CausalMutation CLINVAR Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients. 24611677

2015
dbSNP: rs1209130981
rs1209130981
LAMA2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1211739649
rs1211739649
LAMA2
G 0.700 GeneticVariation CLINVAR LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies. 25663498

2015
dbSNP: rs121913569
rs121913569
LAMA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913569
rs121913569
LAMA2
T 0.700 GeneticVariation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs121913569
rs121913569
LAMA2
T 0.700 GeneticVariation CLINVAR Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. 7550355

1995
dbSNP: rs121913572
rs121913572
LAMA2
T 0.700 CausalMutation CLINVAR Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients. 24611677

2015
dbSNP: rs121913572
rs121913572
LAMA2
T 0.700 CausalMutation CLINVAR Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. 20207543

2010
dbSNP: rs121913573
rs121913573
LAMA2
0.700 GeneticVariation UNIPROT Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients. 24611677

2015
dbSNP: rs121913573
rs121913573
LAMA2
0.700 GeneticVariation UNIPROT Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. 27234031

2017
dbSNP: rs121913573
rs121913573
LAMA2
0.700 GeneticVariation UNIPROT Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 12552556

2003