rs3776082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3776082(A;A) |
Make rs3776082(A;G) |
Make rs3776082(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 150164482 |
is a | snp |
is | mentioned by |
dbSNP | rs3776082 |
dbSNP (classic) | rs3776082 |
ClinGen | rs3776082 |
ebi | rs3776082 |
HLI | rs3776082 |
Exac | rs3776082 |
Gnomad | rs3776082 |
Varsome | rs3776082 |
LitVar | rs3776082 |
Map | rs3776082 |
PheGenI | rs3776082 |
Biobank | rs3776082 |
1000 genomes | rs3776082 |
hgdp | rs3776082 |
ensembl | rs3776082 |
geneview | rs3776082 |
scholar | rs3776082 |
rs3776082 | |
pharmgkb | rs3776082 |
gwascentral | rs3776082 |
openSNP | rs3776082 |
23andMe | rs3776082 |
SNPshot | rs3776082 |
SNPdbe | rs3776082 |
MSV3d | rs3776082 |
GWAS Ctlg | rs3776082 |
GMAF | 0.494 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23918153] Single nucleotide polymorphisms of caudal type homeobox 1 and 2 are associated with Barrett's esophagus