{{Rsnum
|rsid=11568821
|Gene=PDCD1
|Chromosome=2
|position=241851760
|Orientation=plus
|GMAF=0.04821
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PDCD1
}}[http://jcem.endojournals.org/cgi/content/abstract/92/8/3338 Abstract]

intronic snp associated with systemic [[lupus]] erythematosus and [[rheumatoid arthritis]].

{{PMID Auto
|PMID=19581275
|Title=Association between a polymorphism in the human programmed death-1 (PD-1) gene and CMV infection after kidney transplantation
}}

{{PMID Auto
|PMID=15657875
|Title=Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus.
|OA=1
}}

{{PMID Auto
|PMID=17535987
|Title=Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
}}

{{PMID Auto
|PMID=18045485
|Title=The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=18401354
|Title=Analysis of the functional relevance of a putative regulatory SNP of PDCD1, PD1.3, associated with systemic lupus erythematosus.
}}

{{PMID Auto
|PMID=18456185
|Title=Genetics and genomics of primary biliary cirrhosis.
|OA=1
}}

{{PMID Auto
|PMID=19234630
|Title=PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome.
|OA=1
}}

{{PMID Auto
|PMID=23628397
|Title=Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients
}}

{{PMID Auto
|PMID=24804191
|Title=A Promoter Region Polymorphism in PDCD-1 Gene Is Associated with Risk of Rheumatoid Arthritis in the Han Chinese Population of Southeastern China
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}