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rs7869487

From SNPedia

Orientationplus
Stabilizedplus
Make rs7869487(C;C)
Make rs7869487(C;T)
Make rs7869487(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position114818634
is asnp
is mentioned by
dbSNPrs7869487
ebirs7869487
HLIrs7869487
Exacrs7869487
Varsomers7869487
Maprs7869487
PheGenIrs7869487
hapmaprs7869487
1000 genomesrs7869487
hgdprs7869487
ensemblrs7869487
gopubmedrs7869487
geneviewrs7869487
scholarrs7869487
googlers7869487
pharmgkbrs7869487
gwascentralrs7869487
openSNPrs7869487
23andMers7869487
23andMe allrs7869487
SNP Nexus

SNPshotrs7869487
SNPdbers7869487
MSV3drs7869487
GWAS Ctlgrs7869487
GMAF0.2585
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM612259
DescINFLAMMATORY BOWEL DISEASE 16; IBD16
Variant
Relatedalso
[PMID 17663424OA-icon.png] TNFSF15 is an ethnic-specific IBD gene.

[PMID 19174806] TNFSF15 polymorphisms are associated with susceptibility to inflammatory bowel disease in a new European cohort.

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


[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 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