Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1415944134
rs1415944134
LAMA2
CG 0.700 GeneticVariation CLINVAR Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. 30301903

2018
dbSNP: rs914395925
rs914395925
LAMA2 ; LOC102723409
G 0.700 GeneticVariation CLINVAR LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes. 30055037

2018
dbSNP: rs914395925
rs914395925
LAMA2 ; LOC102723409
G 0.700 GeneticVariation CLINVAR High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency. 24225367

2014
dbSNP: rs1415944134
rs1415944134
LAMA2
CG 0.700 GeneticVariation CLINVAR Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. 20207543

2010
dbSNP: rs121913574
rs121913574
LAMA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913575
rs121913575
LAMA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913576
rs121913576
LAMA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554269966
rs1554269966
LAMA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs776548207
rs776548207
LAMA2
C 0.700 GeneticVariation CLINVAR