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rs736289

From SNPedia

Orientationplus
Stabilizedplus
Make rs736289(C;C)
Make rs736289(C;T)
Make rs736289(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position33266156
is asnp
is mentioned by
dbSNPrs736289
dbSNP (classic)rs736289
ClinGenrs736289
ebirs736289
HLIrs736289
Exacrs736289
Gnomadrs736289
Varsomers736289
LitVarrs736289
Maprs736289
PheGenIrs736289
Biobankrs736289
1000 genomesrs736289
hgdprs736289
ensemblrs736289
geneviewrs736289
scholarrs736289
googlers736289
pharmgkbrs736289
gwascentralrs736289
openSNPrs736289
23andMers736289
SNPshotrs736289
SNPdbers736289
MSV3drs736289
GWAS Ctlgrs736289
GMAF0.4614
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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 T
P-val 9E-9
Odds Ratio 1.0600 [1.02-1.11]


[PMID 21247474OA-icon.png] Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.