rs1800692
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1800692(C;C) |
| Make rs1800692(C;T) |
| Make rs1800692(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6333180 |
| Gene | TNFRSF1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800692 |
| dbSNP (classic) | rs1800692 |
| ClinGen | rs1800692 |
| ebi | rs1800692 |
| HLI | rs1800692 |
| Exac | rs1800692 |
| Gnomad | rs1800692 |
| Varsome | rs1800692 |
| LitVar | rs1800692 |
| Map | rs1800692 |
| PheGenI | rs1800692 |
| Biobank | rs1800692 |
| 1000 genomes | rs1800692 |
| hgdp | rs1800692 |
| ensembl | rs1800692 |
| geneview | rs1800692 |
| scholar | rs1800692 |
| rs1800692 | |
| pharmgkb | rs1800692 |
| gwascentral | rs1800692 |
| openSNP | rs1800692 |
| 23andMe | rs1800692 |
| SNPshot | rs1800692 |
| SNPdbe | rs1800692 |
| MSV3d | rs1800692 |
| GWAS Ctlg | rs1800692 |
| GMAF | 0.3081 |
| Max Magnitude | 0 |
[PMID 23269568] The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease
[PMID 17705862
] Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples.
[PMID 19356949] Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies.
[PMID 23505244] Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene.
