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rs3812863

From SNPedia

Orientationplus
Stabilizedplus
Make rs3812863(A;A)
Make rs3812863(A;G)
Make rs3812863(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27971131
GeneCDX2
is asnp
is mentioned by
dbSNPrs3812863
ebirs3812863
HLIrs3812863
Exacrs3812863
Varsomers3812863
Maprs3812863
PheGenIrs3812863
hapmaprs3812863
1000 genomesrs3812863
hgdprs3812863
ensemblrs3812863
gopubmedrs3812863
geneviewrs3812863
scholarrs3812863
googlers3812863
pharmgkbrs3812863
gwascentralrs3812863
openSNPrs3812863
23andMers3812863
23andMe allrs3812863
SNP Nexus

SNPshotrs3812863
SNPdbers3812863
MSV3drs3812863
GWAS Ctlgrs3812863
GMAF0.4348
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23918153OA-icon.png] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus