rs17864678
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17864678(A;A) |
Make rs17864678(A;T) |
Make rs17864678(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233635964 |
Gene | UGT1A8, UGT1A10 |
is a | snp |
is | mentioned by |
dbSNP | rs17864678 |
dbSNP (classic) | rs17864678 |
ClinGen | rs17864678 |
ebi | rs17864678 |
HLI | rs17864678 |
Exac | rs17864678 |
Gnomad | rs17864678 |
Varsome | rs17864678 |
LitVar | rs17864678 |
Map | rs17864678 |
PheGenI | rs17864678 |
Biobank | rs17864678 |
1000 genomes | rs17864678 |
hgdp | rs17864678 |
ensembl | rs17864678 |
geneview | rs17864678 |
scholar | rs17864678 |
rs17864678 | |
pharmgkb | rs17864678 |
gwascentral | rs17864678 |
openSNP | rs17864678 |
23andMe | rs17864678 |
SNPshot | rs17864678 |
SNPdbe | rs17864678 |
MSV3d | rs17864678 |
GWAS Ctlg | rs17864678 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24822274] The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and gene–environment interactions