rs3811021
Orientation | minus |
Stabilized | minus |
Make rs3811021(C;C) |
Make rs3811021(C;T) |
Make rs3811021(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 113814041 |
Gene | AP4B1-AS1, PTPN22, RSBN1 |
is a | snp |
is | mentioned by |
dbSNP | rs3811021 |
dbSNP (classic) | rs3811021 |
ClinGen | rs3811021 |
ebi | rs3811021 |
HLI | rs3811021 |
Exac | rs3811021 |
Gnomad | rs3811021 |
Varsome | rs3811021 |
LitVar | rs3811021 |
Map | rs3811021 |
PheGenI | rs3811021 |
Biobank | rs3811021 |
1000 genomes | rs3811021 |
hgdp | rs3811021 |
ensembl | rs3811021 |
geneview | rs3811021 |
scholar | rs3811021 |
rs3811021 | |
pharmgkb | rs3811021 |
gwascentral | rs3811021 |
openSNP | rs3811021 |
23andMe | rs3811021 |
SNPshot | rs3811021 |
SNPdbe | rs3811021 |
MSV3d | rs3811021 |
GWAS Ctlg | rs3811021 |
GMAF | 0.1589 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19503742] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
[PMID 16175503] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
[PMID 16478714] Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans.
[PMID 17934143] Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.
[PMID 18075792] PTPN22: its role in SLE and autoimmunity.
[PMID 18341666] Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.
[PMID 18466461] Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.
[PMID 18466531] Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.
[PMID 18466575] Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis.
[PMID 19180477] Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.
[PMID 24386393] Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves' Disease in a Chinese Han Population