Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906644
rs387906644
LAMB2
0.800 GeneticVariation UNIPROT A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome. 21236492

2011
dbSNP: rs387906644
rs387906644
LAMB2
0.800 GeneticVariation UNIPROT Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. 20798252

2010
dbSNP: rs387906644
rs387906644
LAMB2
C 0.800 CausalMutation CLINVAR