Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11218708
rs11218708 		A 0.710 GeneticVariation GWASCAT Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population. 29857070

2018
dbSNP: rs11218708
rs11218708 		0.710 GeneticVariation BEFREE We identified rs11218708 (P = 3.1 × 10<sup>-8</sup>, odds ratio = 1.54) at chromosome locus 11q24.1 as significantly associated with PV. 29857070

2018