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rs10889569

From SNPedia

Orientationplus
Stabilizedplus
Make rs10889569(A;A)
Make rs10889569(A;T)
Make rs10889569(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position65620511
GeneLEPR
is asnp
is mentioned by
dbSNPrs10889569
ebirs10889569
HLIrs10889569
Exacrs10889569
Varsomers10889569
Maprs10889569
PheGenIrs10889569
hapmaprs10889569
1000 genomesrs10889569
hgdprs10889569
ensemblrs10889569
gopubmedrs10889569
geneviewrs10889569
scholarrs10889569
googlers10889569
pharmgkbrs10889569
gwascentralrs10889569
openSNPrs10889569
23andMers10889569
23andMe allrs10889569
SNP Nexus

SNPshotrs10889569
SNPdbers10889569
MSV3drs10889569
GWAS Ctlgrs10889569
GMAF0.4366
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23844046OA-icon.png]
Trait C-reactive protein
Title Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?
Risk Allele T
P-val 9E-9
Odds Ratio .05 [NR] unit increase