Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs151190720
rs151190720
LAMC2
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease 		T 0.700 GeneticVariation CLINVAR Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa? 11231327

2001