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rs3810936

From SNPedia

Orientationplus
Stabilizedplus
Make rs3810936(C;C)
Make rs3810936(C;T)
Make rs3810936(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position114790605
GeneTNFSF15
is asnp
is mentioned by
dbSNPrs3810936
ebirs3810936
HLIrs3810936
Exacrs3810936
Varsomers3810936
Maprs3810936
PheGenIrs3810936
hapmaprs3810936
1000 genomesrs3810936
hgdprs3810936
ensemblrs3810936
gopubmedrs3810936
geneviewrs3810936
scholarrs3810936
googlers3810936
pharmgkbrs3810936
gwascentralrs3810936
openSNPrs3810936
23andMers3810936
23andMe allrs3810936
SNP Nexus

SNPshotrs3810936
SNPdbers3810936
MSV3drs3810936
GWAS Ctlgrs3810936
GMAF0.3058
Max Magnitude
? (C;C) (C;T) (T;T) 28
Associated with increased risk for Crohn's disease in a study of 380 Korean patients.[PMID 18422820]
OMIM612259
DescINFLAMMATORY BOWEL DISEASE 16; IBD16
Variant
Relatedalso
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele C
P-val 1E-15
Odds Ratio 1.2100 [1.15-1.27]


[PMID 17663424OA-icon.png] TNFSF15 is an ethnic-specific IBD gene.


[PMID 19262684OA-icon.png] IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein.


[PMID 23388546] Association study of 71 European Crohn's disease susceptibility loci in a Japanese population


[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 26200500] Association of Genetic Variations in TNFSF15 With Acute Anterior Uveitis in Chinese Han


[PMID 25501099OA-icon.png] Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population