rs6714486
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6714486(A;A) |
Make rs6714486(A;T) |
Make rs6714486(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 233671659 |
Gene | UGT1A8, UGT1A9, UGT1A10 |
is a | snp |
is | mentioned by |
dbSNP | rs6714486 |
dbSNP (classic) | rs6714486 |
ClinGen | rs6714486 |
ebi | rs6714486 |
HLI | rs6714486 |
Exac | rs6714486 |
Gnomad | rs6714486 |
Varsome | rs6714486 |
LitVar | rs6714486 |
Map | rs6714486 |
PheGenI | rs6714486 |
Biobank | rs6714486 |
1000 genomes | rs6714486 |
hgdp | rs6714486 |
ensembl | rs6714486 |
geneview | rs6714486 |
scholar | rs6714486 |
rs6714486 | |
pharmgkb | rs6714486 |
gwascentral | rs6714486 |
openSNP | rs6714486 |
23andMe | rs6714486 |
SNPshot | rs6714486 |
SNPdbe | rs6714486 |
MSV3d | rs6714486 |
GWAS Ctlg | rs6714486 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 28524801] Association of UGT2B7, UGT1A9, ABCG2, and IL23R polymorphisms with rejection risk in kidney transplant patients.