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rs2032314

From SNPedia

Orientationplus
Stabilizedplus
Make rs2032314(C;C)
Make rs2032314(C;T)
Make rs2032314(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position33982222
is asnp
is mentioned by
dbSNPrs2032314
ebirs2032314
HLIrs2032314
Exacrs2032314
Varsomers2032314
Maprs2032314
PheGenIrs2032314
hapmaprs2032314
1000 genomesrs2032314
hgdprs2032314
ensemblrs2032314
gopubmedrs2032314
geneviewrs2032314
scholarrs2032314
googlers2032314
pharmgkbrs2032314
gwascentralrs2032314
openSNPrs2032314
23andMers2032314
23andMe allrs2032314
SNP Nexus

SNPshotrs2032314
SNPdbers2032314
MSV3drs2032314
GWAS Ctlgrs2032314
GMAF0.1864
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 8E-10
Odds Ratio .15 [0.087-0.221] unit increase