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rs10421768

From SNPedia

Orientationplus
Stabilizedplus
Make rs10421768(A;A)
Make rs10421768(A;G)
Make rs10421768(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35281996
GeneHAMP
is asnp
is mentioned by
dbSNPrs10421768
ebirs10421768
HLIrs10421768
Exacrs10421768
Varsomers10421768
Maprs10421768
PheGenIrs10421768
hapmaprs10421768
1000 genomesrs10421768
hgdprs10421768
ensemblrs10421768
gopubmedrs10421768
geneviewrs10421768
scholarrs10421768
googlers10421768
pharmgkbrs10421768
gwascentralrs10421768
openSNPrs10421768
23andMers10421768
23andMe allrs10421768
SNP Nexus

SNPshotrs10421768
SNPdbers10421768
MSV3drs10421768
GWAS Ctlgrs10421768
GMAF0.1547
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19734422OA-icon.png] Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major