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rs267734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs267734(A;G)
Make rs267734(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position150979001
is asnp
is mentioned by
dbSNPrs267734
dbSNP (classic)rs267734
ClinGenrs267734
ebirs267734
HLIrs267734
Exacrs267734
Gnomadrs267734
Varsomers267734
LitVarrs267734
Maprs267734
PheGenIrs267734
Biobankrs267734
1000 genomesrs267734
hgdprs267734
ensemblrs267734
geneviewrs267734
scholarrs267734
googlers267734
pharmgkbrs267734
gwascentralrs267734
openSNPrs267734
23andMers267734
SNPshotrs267734
SNPdbers267734
MSV3drs267734
GWAS Ctlgrs267734
GMAF0.09826
Max Magnitude0
? (A;A) (A;G) (G;G) 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 1E-12
Odds Ratio 0.01 [0.004-0.016] ml/min/1.73m2 increase