Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553266871
rs1553266871
LAMC2
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease 		A 0.700 GeneticVariation CLINVAR Laminin-5 mutational analysis in an Italian cohort of patients with junctional epidermolysis bullosa. 15373767

2004