rs717746
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs717746(A;A) |
Make rs717746(A;C) |
Make rs717746(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 150176995 |
Gene | CDX1 |
is a | snp |
is | mentioned by |
dbSNP | rs717746 |
dbSNP (classic) | rs717746 |
ClinGen | rs717746 |
ebi | rs717746 |
HLI | rs717746 |
Exac | rs717746 |
Gnomad | rs717746 |
Varsome | rs717746 |
LitVar | rs717746 |
Map | rs717746 |
PheGenI | rs717746 |
Biobank | rs717746 |
1000 genomes | rs717746 |
hgdp | rs717746 |
ensembl | rs717746 |
geneview | rs717746 |
scholar | rs717746 |
rs717746 | |
pharmgkb | rs717746 |
gwascentral | rs717746 |
openSNP | rs717746 |
23andMe | rs717746 |
SNPshot | rs717746 |
SNPdbe | rs717746 |
MSV3d | rs717746 |
GWAS Ctlg | rs717746 |
GMAF | 0.4706 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23918153] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus