rs9469220, None

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
0.710 GeneticVariation GWASCAT Subtype-specific inherited predisposition to pemphigus in the Chinese population. 30230522 2019
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
0.710 GeneticVariation BEFREE The strongest associated single-nucleotide polymorphisms are in the human leucocyte antigen (HLA) region: rs70993900 (PV; P = 1·5 × 10<sup>-45</sup> ) and rs9469220 (PF; P = 1·1 × 10<sup>-8</sup> ). 30230522 2019
Pemphigus
CUI: C0030807
Disease: Pemphigus
0.700 GeneticVariation GWASCAT Subtype-specific inherited predisposition to pemphigus in the Chinese population. 30230522 2019
Narcolepsy
CUI: C0027404
Disease: Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
Pemphigus Foliaceus
CUI: C0263313
Disease: Pemphigus Foliaceus
0.010 GeneticVariation BEFREE The strongest associated single-nucleotide polymorphisms are in the human leucocyte antigen (HLA) region: rs70993900 (PV; P = 1·5 × 10<sup>-45</sup> ) and rs9469220 (PF; P = 1·1 × 10<sup>-8</sup> ). 30230522 2019