rs4460629
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4460629(C;C) |
Make rs4460629(C;T) |
Make rs4460629(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 155162859 |
is a | snp |
is | mentioned by |
dbSNP | rs4460629 |
dbSNP (classic) | rs4460629 |
ClinGen | rs4460629 |
ebi | rs4460629 |
HLI | rs4460629 |
Exac | rs4460629 |
Gnomad | rs4460629 |
Varsome | rs4460629 |
LitVar | rs4460629 |
Map | rs4460629 |
PheGenI | rs4460629 |
Biobank | rs4460629 |
1000 genomes | rs4460629 |
hgdp | rs4460629 |
ensembl | rs4460629 |
geneview | rs4460629 |
scholar | rs4460629 |
rs4460629 | |
pharmgkb | rs4460629 |
gwascentral | rs4460629 |
openSNP | rs4460629 |
23andMe | rs4460629 |
SNPshot | rs4460629 |
SNPdbe | rs4460629 |
MSV3d | rs4460629 |
GWAS Ctlg | rs4460629 |
GMAF | 0.3554 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22938415] Association of genetic polymorphisms at 1q22 but not 10q23 with gastric cancer in a southern Chinese population
[PMID 22740136] Association of 10q23 with colorectal cancer in a Chinese population.