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rs111033557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs111033557(A;A)
Make rs111033557(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position26090939
GeneHFE
is asnp
is mentioned by
dbSNPrs111033557
ClinGenrs111033557
ebirs111033557
HLIrs111033557
Exacrs111033557
Varsomers111033557
Maprs111033557
PheGenIrs111033557
hapmaprs111033557
1000 genomesrs111033557
hgdprs111033557
ensemblrs111033557
gopubmedrs111033557
geneviewrs111033557
scholarrs111033557
googlers111033557
pharmgkbrs111033557
gwascentralrs111033557
openSNPrs111033557
23andMers111033557
23andMe allrs111033557
SNP Nexus

SNPshotrs111033557
SNPdbers111033557
MSV3drs111033557
GWAS Ctlgrs111033557
Merged fromRs28934890
Max Magnitude0
OMIM613609
Desc
Variant0006
Relatedalso
ClinVar
Risk rs111033557(A;A)
Alt rs111033557(A;A)
Reference Rs111033557(G;G)
Significance Non-pathogenic
Disease HFE POLYMORPHISM
Variation info
Gene HFE
CLNDBN HFE POLYMORPHISM
Reversed 0
HGVS NC_000006.11:g.26091167G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000000033.3,