rs4276913
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4276913(A;A) |
Make rs4276913(A;G) |
Make rs4276913(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 155159197 |
is a | snp |
is | mentioned by |
dbSNP | rs4276913 |
dbSNP (classic) | rs4276913 |
ClinGen | rs4276913 |
ebi | rs4276913 |
HLI | rs4276913 |
Exac | rs4276913 |
Gnomad | rs4276913 |
Varsome | rs4276913 |
LitVar | rs4276913 |
Map | rs4276913 |
PheGenI | rs4276913 |
Biobank | rs4276913 |
1000 genomes | rs4276913 |
hgdp | rs4276913 |
ensembl | rs4276913 |
geneview | rs4276913 |
scholar | rs4276913 |
rs4276913 | |
pharmgkb | rs4276913 |
gwascentral | rs4276913 |
openSNP | rs4276913 |
23andMe | rs4276913 |
SNPshot | rs4276913 |
SNPdbe | rs4276913 |
MSV3d | rs4276913 |
GWAS Ctlg | rs4276913 |
GMAF | 0.4986 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19924550] A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer