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rs3776082

From SNPedia

Orientationplus
Stabilizedplus
Make rs3776082(A;A)
Make rs3776082(A;G)
Make rs3776082(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150164482
is asnp
is mentioned by
dbSNPrs3776082
ebirs3776082
HLIrs3776082
Exacrs3776082
Varsomers3776082
Maprs3776082
PheGenIrs3776082
hapmaprs3776082
1000 genomesrs3776082
hgdprs3776082
ensemblrs3776082
gopubmedrs3776082
geneviewrs3776082
scholarrs3776082
googlers3776082
pharmgkbrs3776082
gwascentralrs3776082
openSNPrs3776082
23andMers3776082
23andMe allrs3776082
SNP Nexus

SNPshotrs3776082
SNPdbers3776082
MSV3drs3776082
GWAS Ctlgrs3776082
GMAF0.494
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