rs6478108
Orientation | plus |
Stabilized | plus |
Make rs6478108(C;C) |
Make rs6478108(C;T) |
Make rs6478108(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 114796423 |
Gene | TNFSF15 |
is a | snp |
is | mentioned by |
dbSNP | rs6478108 |
dbSNP (classic) | rs6478108 |
ClinGen | rs6478108 |
ebi | rs6478108 |
HLI | rs6478108 |
Exac | rs6478108 |
Gnomad | rs6478108 |
Varsome | rs6478108 |
LitVar | rs6478108 |
Map | rs6478108 |
PheGenI | rs6478108 |
Biobank | rs6478108 |
1000 genomes | rs6478108 |
hgdp | rs6478108 |
ensembl | rs6478108 |
geneview | rs6478108 |
scholar | rs6478108 |
rs6478108 | |
pharmgkb | rs6478108 |
gwascentral | rs6478108 |
openSNP | rs6478108 |
23andMe | rs6478108 |
SNPshot | rs6478108 |
SNPdbe | rs6478108 |
MSV3d | rs6478108 |
GWAS Ctlg | rs6478108 |
GMAF | 0.3072 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Associated with increased risk for Crohn's disease in a study of 380 Korean patients.[PMID 18422820]
This SNP is associated with greater susceptibility to leprosy in Asians, according to the 23andMe blog. The risk allele is T, and the odds ratio is 1.37.
The TNFSF15 gene encodes a cytokine protein in the tumor necrosis factor (TNF) family.
GWAS snp | |
---|---|
PMID | [PMID 20018961] |
Trait | Leprosy |
Title | Genomewide Association Study of Leprosy |
Risk Allele | A |
P-val | 3E-21 |
Odds Ratio | 1.37 [1.28-1.46] |
[PMID 17663424] TNFSF15 is an ethnic-specific IBD gene.
[PMID 18758464] Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.
[PMID 19174806] TNFSF15 polymorphisms are associated with susceptibility to inflammatory bowel disease in a new European cohort.
[PMID 19262684] IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein.
[PMID 19543369] Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis.
[PMID 22684480] Identifying and testing candidate genetic polymorphisms in the irritable bowel syndrome (IBS): association with TNFSF15 and TNFalpha
[PMID 24269700] Genetic risk and protective factors of TNFSF15 gene variants detected using single nucleotide polymorphisms in Hungarians with psoriasis and psoriatic arthritis
[PMID 25028192] Associations between TNFSF15 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: A meta-analysis
[PMID 26398853] Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans
[PMID 25501099] Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population
[PMID 31615448] Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis.
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d