rs10891246
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10891246(A;A) |
Make rs10891246(A;G) |
Make rs10891246(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 111299815 |
Gene | COLCA1, COLCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs10891246 |
dbSNP (classic) | rs10891246 |
ClinGen | rs10891246 |
ebi | rs10891246 |
HLI | rs10891246 |
Exac | rs10891246 |
Gnomad | rs10891246 |
Varsome | rs10891246 |
LitVar | rs10891246 |
Map | rs10891246 |
PheGenI | rs10891246 |
Biobank | rs10891246 |
1000 genomes | rs10891246 |
hgdp | rs10891246 |
ensembl | rs10891246 |
geneview | rs10891246 |
scholar | rs10891246 |
rs10891246 | |
pharmgkb | rs10891246 |
gwascentral | rs10891246 |
openSNP | rs10891246 |
23andMe | rs10891246 |
SNPshot | rs10891246 |
SNPdbe | rs10891246 |
MSV3d | rs10891246 |
GWAS Ctlg | rs10891246 |
GMAF | 0.298 |
Max Magnitude | 0 |
[PMID 24256810] Identification and Characterization of Functional Risk Variants for Colorectal Cancer Mapping to Chromosome 11q23.1