rs26653
| Orientation | plus |
| Stabilized | plus |
| Make rs26653(C;C) |
| Make rs26653(C;G) |
| Make rs26653(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 96803547 |
| Gene | ERAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs26653 |
| dbSNP (classic) | rs26653 |
| ClinGen | rs26653 |
| ebi | rs26653 |
| HLI | rs26653 |
| Exac | rs26653 |
| Gnomad | rs26653 |
| Varsome | rs26653 |
| LitVar | rs26653 |
| Map | rs26653 |
| PheGenI | rs26653 |
| Biobank | rs26653 |
| 1000 genomes | rs26653 |
| hgdp | rs26653 |
| ensembl | rs26653 |
| geneview | rs26653 |
| scholar | rs26653 |
| rs26653 | |
| pharmgkb | rs26653 |
| gwascentral | rs26653 |
| openSNP | rs26653 |
| 23andMe | rs26653 |
| SNPshot | rs26653 |
| SNPdbe | rs26653 |
| MSV3d | rs26653 |
| GWAS Ctlg | rs26653 |
| GMAF | 0.4284 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19404951] Association of a specific ERAP1/ARTS1 haplotype with disease susceptibility in ankylosing spondylitis
[PMID 16251468
] Survey of allelic expression using EST mining.
[PMID 19692350] Investigating the genetic association between ERAP1 and ankylosing spondylitis.
[PMID 21865284] ERAP1 polymorphisms and haplotypes are associated with ankylosing spondylitis susceptibility and functional severity in a Spanish population.
[PMID 23864143] A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population
[PMID 22931917] Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C*06.
[PMID 28083613] Single Nucleotide Polymorphisms of the ERAP1 Gene and Risk of NSCLC: A Comparison of Genetically Distant Populations, Chinese and Caucasian.
[PMID 28867178] Associations of ERAP1 coding variants and domain specific interaction with HLA-C∗06 in the early onset psoriasis patients of India.
[PMID 29183862] The association of ERAP1 and ERAP2 single nucleotide polymorphisms and their haplotypes with psoriasis vulgaris is dependent on the presence or absence of the HLA-C∗06:02 allele and age at disease onset.
