Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554227092
rs1554227092
LAMA2
CCT 0.700 GeneticVariation CLINVAR Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. 9674786

1998