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rs2698530

From SNPedia

Orientationplus
Stabilizedplus
Make rs2698530(A;A)
Make rs2698530(A;C)
Make rs2698530(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position64276761
is asnp
is mentioned by
dbSNPrs2698530
ebirs2698530
HLIrs2698530
Exacrs2698530
Varsomers2698530
Maprs2698530
PheGenIrs2698530
hapmaprs2698530
1000 genomesrs2698530
hgdprs2698530
ensemblrs2698530
gopubmedrs2698530
geneviewrs2698530
scholarrs2698530
googlers2698530
pharmgkbrs2698530
gwascentralrs2698530
openSNPrs2698530
23andMers2698530
23andMe allrs2698530
SNP Nexus

SNPshotrs2698530
SNPdbers2698530
MSV3drs2698530
GWAS Ctlgrs2698530
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21483845OA-icon.png]
Trait Iron status biomarkers
Title Genome-wide association study identifies genetic loci associated with iron deficiency.
Risk Allele C
P-val 4E-6
Odds Ratio 20.00 [NR] unit decrease