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rs2769264

From SNPedia

Orientationminus
Stabilizedminus
Make rs2769264(A;A)
Make rs2769264(A;C)
Make rs2769264(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position151372265
GeneSELENBP1
is asnp
is mentioned by
dbSNPrs2769264
dbSNP (classic)rs2769264
ClinGenrs2769264
ebirs2769264
HLIrs2769264
Exacrs2769264
Gnomadrs2769264
Varsomers2769264
LitVarrs2769264
Maprs2769264
PheGenIrs2769264
Biobankrs2769264
1000 genomesrs2769264
hgdprs2769264
ensemblrs2769264
geneviewrs2769264
scholarrs2769264
googlers2769264
pharmgkbrs2769264
gwascentralrs2769264
openSNPrs2769264
23andMers2769264
SNPshotrs2769264
SNPdbers2769264
MSV3drs2769264
GWAS Ctlgrs2769264
GMAF0.27
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Cu levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele G
P-val 3E-20
Odds Ratio .31 [0.25-0.38] unit increase


[PMID 18426996OA-icon.png] Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.