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rs717746

From SNPedia

Orientationminus
Stabilizedminus
Make rs717746(A;A)
Make rs717746(A;C)
Make rs717746(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position150176995
GeneCDX1
is asnp
is mentioned by
dbSNPrs717746
ebirs717746
HLIrs717746
Exacrs717746
Varsomers717746
Maprs717746
PheGenIrs717746
hapmaprs717746
1000 genomesrs717746
hgdprs717746
ensemblrs717746
gopubmedrs717746
geneviewrs717746
scholarrs717746
googlers717746
pharmgkbrs717746
gwascentralrs717746
openSNPrs717746
23andMers717746
23andMe allrs717746
SNP Nexus

SNPshotrs717746
SNPdbers717746
MSV3drs717746
GWAS Ctlgrs717746
GMAF0.4706
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 23918153OA-icon.png] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus