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rs733175

From SNPedia

Orientationplus
Stabilizedplus
Make rs733175(C;C)
Make rs733175(C;T)
Make rs733175(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position10048517
is asnp
is mentioned by
dbSNPrs733175
ebirs733175
HLIrs733175
Exacrs733175
Varsomers733175
Maprs733175
PheGenIrs733175
hapmaprs733175
1000 genomesrs733175
hgdprs733175
ensemblrs733175
gopubmedrs733175
geneviewrs733175
scholarrs733175
googlers733175
pharmgkbrs733175
gwascentralrs733175
openSNPrs733175
23andMers733175
23andMe allrs733175
SNP Nexus

SNPshotrs733175
SNPdbers733175
MSV3drs733175
GWAS Ctlgrs733175
GMAF0.2948
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20589538] Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson's Disease

GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000005
Odds Ratio 1.3700 None


[PMID 19260141OA-icon.png] Genome-wide association study of biochemical traits in Korcula Island, Croatia.


[PMID 20162742OA-icon.png] Predictive value of 8 genetic loci for serum uric acid concentration.


[PMID 20162743OA-icon.png] Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series.


[PMID 20162745OA-icon.png] Association of nephrolithiasis and gene for glucose transporter type 9 (SLC2A9): study of 145 patients.