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rs11104870

From SNPedia

Orientationplus
Stabilizedplus
Make rs11104870(C;C)
Make rs11104870(C;T)
Make rs11104870(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position88435517
is asnp
is mentioned by
dbSNPrs11104870
ebirs11104870
HLIrs11104870
Exacrs11104870
Varsomers11104870
Maprs11104870
PheGenIrs11104870
hapmaprs11104870
1000 genomesrs11104870
hgdprs11104870
ensemblrs11104870
gopubmedrs11104870
geneviewrs11104870
scholarrs11104870
googlers11104870
pharmgkbrs11104870
gwascentralrs11104870
openSNPrs11104870
23andMers11104870
23andMe allrs11104870
SNP Nexus

SNPshotrs11104870
SNPdbers11104870
MSV3drs11104870
GWAS Ctlgrs11104870
GMAF0.4192
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 C
P-val 6E-11
Odds Ratio .01 [0.0091-0.0169] unit increase