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rs5749446

From SNPedia

Orientationplus
Stabilizedplus
Make rs5749446(C;C)
Make rs5749446(C;T)
Make rs5749446(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32484598
GeneFBXO7
is asnp
is mentioned by
dbSNPrs5749446
ebirs5749446
HLIrs5749446
Exacrs5749446
Varsomers5749446
Maprs5749446
PheGenIrs5749446
hapmaprs5749446
1000 genomesrs5749446
hgdprs5749446
ensemblrs5749446
gopubmedrs5749446
geneviewrs5749446
scholarrs5749446
googlers5749446
pharmgkbrs5749446
gwascentralrs5749446
openSNPrs5749446
23andMers5749446
23andMe allrs5749446
SNP Nexus

SNPshotrs5749446
SNPdbers5749446
MSV3drs5749446
GWAS Ctlgrs5749446
GMAF0.489
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele T
P-val 3E-13
Odds Ratio .01 [-0.00084-0.01484] unit increase