rs2075674

Orientation

minus

Stabilized

minus

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

Make rs2075674(C;T)

Make rs2075674(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

100627408

Gene

TFR2

is a	snp
is	mentioned by
dbSNP	rs2075674
dbSNP (classic)	rs2075674
ClinGen	rs2075674
ebi	rs2075674
HLI	rs2075674
Exac	rs2075674
Gnomad	rs2075674
Varsome	rs2075674
LitVar	rs2075674
Map	rs2075674
PheGenI	rs2075674
Biobank	rs2075674
1000 genomes	rs2075674
hgdp	rs2075674
ensembl	rs2075674
geneview	rs2075674
scholar	rs2075674
google	rs2075674
pharmgkb	rs2075674
gwascentral	rs2075674
openSNP	rs2075674
23andMe	rs2075674
SNPshot	rs2075674
SNPdbe	rs2075674
MSV3d	rs2075674
GWAS Ctlg	rs2075674

GMAF

0.1538

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 23751596] Association between genetic variations in TFR2 gene and coronary heart disease in Chinese: a case-control study

ClinVar
Risk	rs2075674(T;T)
Alt	rs2075674(T;T)
Reference	Rs2075674(C;C)
Significance	Non-pathogenic
Disease	Hemochromatosis type 3 not specified Hereditary hemochromatosis
Variation	info
Gene	TFR2
CLNDBN	Hemochromatosis type 3 not specified Hereditary hemochromatosis
Reversed	1
HGVS	NC_000007.13:g.100225031G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020542.1, RCV000248610.1, RCV000355274.1,

[PMID 11102989] Molecular analysis of the TFR2 gene: report of a novel polymorphism (1878C>T).