rs11118883
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11118883(A;A) |
Make rs11118883(A;G) |
Make rs11118883(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 221887680 |
Gene | LOC105372950 |
is a | snp |
is | mentioned by |
dbSNP | rs11118883 |
dbSNP (classic) | rs11118883 |
ClinGen | rs11118883 |
ebi | rs11118883 |
HLI | rs11118883 |
Exac | rs11118883 |
Gnomad | rs11118883 |
Varsome | rs11118883 |
LitVar | rs11118883 |
Map | rs11118883 |
PheGenI | rs11118883 |
Biobank | rs11118883 |
1000 genomes | rs11118883 |
hgdp | rs11118883 |
ensembl | rs11118883 |
geneview | rs11118883 |
scholar | rs11118883 |
rs11118883 | |
pharmgkb | rs11118883 |
gwascentral | rs11118883 |
openSNP | rs11118883 |
23andMe | rs11118883 |
SNPshot | rs11118883 |
SNPdbe | rs11118883 |
MSV3d | rs11118883 |
GWAS Ctlg | rs11118883 |
GMAF | 0.214 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22076443] Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13