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rs16864170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16864170(C;C)
Make rs16864170(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position5767748
is asnp
is mentioned by
dbSNPrs16864170
ebirs16864170
HLIrs16864170
Exacrs16864170
Varsomers16864170
Maprs16864170
PheGenIrs16864170
hapmaprs16864170
1000 genomesrs16864170
hgdprs16864170
ensemblrs16864170
gopubmedrs16864170
geneviewrs16864170
scholarrs16864170
googlers16864170
pharmgkbrs16864170
gwascentralrs16864170
openSNPrs16864170
23andMers16864170
23andMe allrs16864170
SNP Nexus

SNPshotrs16864170
SNPdbers16864170
MSV3drs16864170
GWAS Ctlgrs16864170
GMAF0.02663
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20383146OA-icon.png]
Trait Chronic kidney disease
Title New loci associated with kidney function and chronic kidney disease
Risk Allele C
P-val 2E-7
Odds Ratio 1.30 [1.18-1.43]