Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs367543072
rs367543072
B3GALNT2
T 0.800 GeneticVariation CLINVAR Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. 23453667

2013
dbSNP: rs367543072
rs367543072
B3GALNT2
0.800 GeneticVariation UNIPROT Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. 23453667

2013
dbSNP: rs367543072
rs367543072
B3GALNT2
T 0.800 CausalMutation CLINVAR