rs13101785
From SNPedia
Orientation | plus |
Make rs13101785(A;A) |
Make rs13101785(A;T) |
Make rs13101785(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 4 |
Position | 10041291 |
Gene | SLC2A9 |
is a | snp |
is | mentioned by |
dbSNP | rs13101785 |
dbSNP (classic) | rs13101785 |
ClinGen | rs13101785 |
ebi | rs13101785 |
HLI | rs13101785 |
Exac | rs13101785 |
Gnomad | rs13101785 |
Varsome | rs13101785 |
LitVar | rs13101785 |
Map | rs13101785 |
PheGenI | rs13101785 |
Biobank | rs13101785 |
1000 genomes | rs13101785 |
hgdp | rs13101785 |
ensembl | rs13101785 |
geneview | rs13101785 |
scholar | rs13101785 |
rs13101785 | |
pharmgkb | rs13101785 |
gwascentral | rs13101785 |
openSNP | rs13101785 |
23andMe | rs13101785 |
SNPshot | rs13101785 |
SNPdbe | rs13101785 |
MSV3d | rs13101785 |
GWAS Ctlg | rs13101785 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 31016517] Association between SLC2A9 Genetic Variants and Risk of Hyperuricemia in a Uygur Population.