rs111033557

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs111033557(A;A)

Make rs111033557(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

26090939

Gene	HFE, LOC108783645

is a	snp
is	mentioned by
dbSNP	rs111033557
dbSNP (classic)	rs111033557
ClinGen	rs111033557
ebi	rs111033557
HLI	rs111033557
Exac	rs111033557
Gnomad	rs111033557
Varsome	rs111033557
LitVar	rs111033557
Map	rs111033557
PheGenI	rs111033557
Biobank	rs111033557
1000 genomes	rs111033557
hgdp	rs111033557
ensembl	rs111033557
geneview	rs111033557
scholar	rs111033557
google	rs111033557
pharmgkb	rs111033557
gwascentral	rs111033557
openSNP	rs111033557
23andMe	rs111033557
SNPshot	rs111033557
SNPdbe	rs111033557
MSV3d	rs111033557
GWAS Ctlg	rs111033557

Merged from

Rs28934890

Max Magnitude

0

OMIM	613609
Desc
Variant	0006
Related	also

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,