Have questions? Visit https://www.reddit.com/r/SNPedia

rs2687201

From SNPedia

Orientationplus
Stabilizedplus
Make rs2687201(A;A)
Make rs2687201(A;C)
Make rs2687201(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position70879779
is asnp
is mentioned by
dbSNPrs2687201
ebirs2687201
HLIrs2687201
Exacrs2687201
Varsomers2687201
Maprs2687201
PheGenIrs2687201
hapmaprs2687201
1000 genomesrs2687201
hgdprs2687201
ensemblrs2687201
gopubmedrs2687201
geneviewrs2687201
scholarrs2687201
googlers2687201
pharmgkbrs2687201
gwascentralrs2687201
openSNPrs2687201
23andMers2687201
23andMe allrs2687201
SNP Nexus

SNPshotrs2687201
SNPdbers2687201
MSV3drs2687201
GWAS Ctlgrs2687201
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24121790OA-icon.png]
Trait Barrett's esophagus
Title A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
Risk Allele T
P-val 2E-6
Odds Ratio 1.18 [1.10-1.26]


[PMID 25447851OA-icon.png] Polymorphisms Near TBX5 and GDF7 are Associated with Increased Risk for Barrett's Esophagus


[PMID 26377193] A newly identified susceptibility locus near FOXP1 modifies the association of gastroesophageal reflux with Barrett's esophagus