rs74315324

Orientation

minus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs74315324(C;T)

Make rs74315324(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

146018382

Gene

HFE2

is a	snp
is	mentioned by
dbSNP	rs74315324
dbSNP (classic)	rs74315324
ClinGen	rs74315324
ebi	rs74315324
HLI	rs74315324
Exac	rs74315324
Gnomad	rs74315324
Varsome	rs74315324
LitVar	rs74315324
Map	rs74315324
PheGenI	rs74315324
Biobank	rs74315324
1000 genomes	rs74315324
hgdp	rs74315324
ensembl	rs74315324
geneview	rs74315324
scholar	rs74315324
google	rs74315324
pharmgkb	rs74315324
gwascentral	rs74315324
openSNP	rs74315324
23andMe	rs74315324
SNPshot	rs74315324
SNPdbe	rs74315324
MSV3d	rs74315324
GWAS Ctlg	rs74315324

Max Magnitude

0

OMIM	608374
Desc
Variant	0002
Related	also

ClinVar
Risk	rs74315324(T;T)
Alt	rs74315324(T;T)
Reference	Rs74315324(C;C)
Significance	Pathogenic
Disease	Hemochromatosis type 2A
Variation	info
Gene	HFE2
CLNDBN	Hemochromatosis type 2A
Reversed	0
HGVS	NC_000001.10:g.145416631C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002463.5,