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rs10849023

From SNPedia

Orientationplus
Stabilizedplus
Make rs10849023(C;C)
Make rs10849023(C;T)
Make rs10849023(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position4223312
is asnp
is mentioned by
dbSNPrs10849023
ebirs10849023
HLIrs10849023
Exacrs10849023
Varsomers10849023
Maprs10849023
PheGenIrs10849023
hapmaprs10849023
1000 genomesrs10849023
hgdprs10849023
ensemblrs10849023
gopubmedrs10849023
geneviewrs10849023
scholarrs10849023
googlers10849023
pharmgkbrs10849023
gwascentralrs10849023
openSNPrs10849023
23andMers10849023
23andMe allrs10849023
SNP Nexus

SNPshotrs10849023
SNPdbers10849023
MSV3drs10849023
GWAS Ctlgrs10849023
GMAF0.2355
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 8E-12
Odds Ratio .01 [-0.00180-0.01780] unit decrease