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rs28934889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28934889(A;A)
Make rs28934889(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position26090921
GeneHFE
is asnp
is mentioned by
dbSNPrs28934889
ebirs28934889
HLIrs28934889
Exacrs28934889
Varsomers28934889
Maprs28934889
PheGenIrs28934889
hapmaprs28934889
1000 genomesrs28934889
hgdprs28934889
ensemblrs28934889
gopubmedrs28934889
geneviewrs28934889
scholarrs28934889
googlers28934889
pharmgkbrs28934889
gwascentralrs28934889
openSNPrs28934889
23andMers28934889
23andMe allrs28934889
SNP Nexus

SNPshotrs28934889
SNPdbers28934889
MSV3drs28934889
GWAS Ctlgrs28934889
GMAF0.0004591
Max Magnitude0
OMIM235200
DescHFE POLYMORPHISM
Variant0005
Relatedalso
Neighborrs28934890
Distance18
OMIM613609
Desc
Variant0005
Relatedalso
ClinVar
Risk rs28934889(A;A)
Alt rs28934889(A;A)
Reference rs28934889(G;G)
Significance Non-pathogenic
Disease HFE POLYMORPHISM
Variation info
Gene HFE
CLNDBN HFE POLYMORPHISM
Reversed 0
HGVS NC_000006.11:g.26091149G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000032.2,