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rs4821469

From SNPedia

Orientationplus
Stabilizedplus
Make rs4821469(C;C)
Make rs4821469(C;T)
Make rs4821469(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36220399
is asnp
is mentioned by
dbSNPrs4821469
ebirs4821469
HLIrs4821469
Exacrs4821469
Varsomers4821469
Maprs4821469
PheGenIrs4821469
hapmaprs4821469
1000 genomesrs4821469
hgdprs4821469
ensemblrs4821469
gopubmedrs4821469
geneviewrs4821469
scholarrs4821469
googlers4821469
pharmgkbrs4821469
gwascentralrs4821469
openSNPrs4821469
23andMers4821469
23andMe allrs4821469
SNP Nexus

SNPshotrs4821469
SNPdbers4821469
MSV3drs4821469
GWAS Ctlgrs4821469
GMAF0.191
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20532800OA-icon.png]
Trait End-stage renal disease (non-diabetic)
Title Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA
Risk Allele
P-val 2E-19
Odds Ratio 2.86 [2.27-3.57]