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rs4769585

From SNPedia

Orientationplus
Stabilizedplus
Make rs4769585(C;C)
Make rs4769585(C;T)
Make rs4769585(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position27976441
GenePRHOXNB
is asnp
is mentioned by
dbSNPrs4769585
ebirs4769585
HLIrs4769585
Exacrs4769585
Varsomers4769585
Maprs4769585
PheGenIrs4769585
hapmaprs4769585
1000 genomesrs4769585
hgdprs4769585
ensemblrs4769585
gopubmedrs4769585
geneviewrs4769585
scholarrs4769585
googlers4769585
pharmgkbrs4769585
gwascentralrs4769585
openSNPrs4769585
23andMers4769585
23andMe allrs4769585
SNP Nexus

SNPshotrs4769585
SNPdbers4769585
MSV3drs4769585
GWAS Ctlgrs4769585
GMAF0.3168
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23918153OA-icon.png] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus