Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2071286
rs2071286
NOTCH4
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris 		0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012