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rs9366637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9366637(C;T)
Make rs9366637(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position26088870
GeneHFE
is asnp
is mentioned by
dbSNPrs9366637
ebirs9366637
HLIrs9366637
Exacrs9366637
Varsomers9366637
Maprs9366637
PheGenIrs9366637
hapmaprs9366637
1000 genomesrs9366637
hgdprs9366637
ensemblrs9366637
gopubmedrs9366637
geneviewrs9366637
scholarrs9366637
googlers9366637
pharmgkbrs9366637
gwascentralrs9366637
openSNPrs9366637
23andMers9366637
23andMe allrs9366637
SNP Nexus

SNPshotrs9366637
SNPdbers9366637
MSV3drs9366637
GWAS Ctlgrs9366637
GMAF0.2259
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21696736] Plasma ferritin levels, genetic variations in HFE gene, and coronary heart disease in Chinese: A case-control study


[PMID 23792061] Meta-analyses of HFE variants in coronary heart disease


[PMID 26054392OA-icon.png] Natural selection on HFE in Asian populations contributes to enhanced non-heme iron absorption