rs12080929
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12080929(C;C) |
Make rs12080929(C;T) |
Make rs12080929(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 47970476 |
Gene | TRABD2B |
is a | snp |
is | mentioned by |
dbSNP | rs12080929 |
dbSNP (classic) | rs12080929 |
ClinGen | rs12080929 |
ebi | rs12080929 |
HLI | rs12080929 |
Exac | rs12080929 |
Gnomad | rs12080929 |
Varsome | rs12080929 |
LitVar | rs12080929 |
Map | rs12080929 |
PheGenI | rs12080929 |
Biobank | rs12080929 |
1000 genomes | rs12080929 |
hgdp | rs12080929 |
ensembl | rs12080929 |
geneview | rs12080929 |
scholar | rs12080929 |
rs12080929 | |
pharmgkb | rs12080929 |
gwascentral | rs12080929 |
openSNP | rs12080929 |
23andMe | rs12080929 |
SNPshot | rs12080929 |
SNPdbe | rs12080929 |
MSV3d | rs12080929 |
GWAS Ctlg | rs12080929 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26148620] Genetic variants identified by GWAS was associated with colorectal cancer in the Han Chinese population