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rs1531343

From SNPedia

Orientationplus
Stabilizedplus
Make rs1531343(C;C)
Make rs1531343(C;G)
Make rs1531343(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position65781114
GeneRPSAP52
is asnp
is mentioned by
dbSNPrs1531343
dbSNP (classic)rs1531343
ClinGenrs1531343
ebirs1531343
HLIrs1531343
Exacrs1531343
Gnomadrs1531343
Varsomers1531343
LitVarrs1531343
Maprs1531343
PheGenIrs1531343
Biobankrs1531343
1000 genomesrs1531343
hgdprs1531343
ensemblrs1531343
geneviewrs1531343
scholarrs1531343
googlers1531343
pharmgkbrs1531343
gwascentralrs1531343
openSNPrs1531343
23andMers1531343
SNPshotrs1531343
SNPdbers1531343
MSV3drs1531343
GWAS Ctlgrs1531343
GMAF0.1915
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 20581827OA-icon.png]
Trait Type 2 diabetes
Title Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Risk Allele C
P-val 4E-9
Odds Ratio 1.10 [1.07-1.14]

[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


[PMID 23111731] Common variant in the HMGA2 gene increases susceptibility to nephropathy in patients with type 2 diabetes


[PMID 23462794OA-icon.png] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.