rs786204108

Orientation

minus

Stabilized

minus

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

Make rs786204108(C;C)

Make rs786204108(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

100626866

Gene

TFR2

is a	snp
is	mentioned by
dbSNP	rs786204108
dbSNP (classic)	rs786204108
ClinGen	rs786204108
ebi	rs786204108
HLI	rs786204108
Exac	rs786204108
Gnomad	rs786204108
Varsome	rs786204108
LitVar	rs786204108
Map	rs786204108
PheGenI	rs786204108
Biobank	rs786204108
1000 genomes	rs786204108
hgdp	rs786204108
ensembl	rs786204108
geneview	rs786204108
scholar	rs786204108
google	rs786204108
pharmgkb	rs786204108
gwascentral	rs786204108
openSNP	rs786204108
23andMe	rs786204108
SNPshot	rs786204108
SNPdbe	rs786204108
MSV3d	rs786204108
GWAS Ctlg	rs786204108

Max Magnitude

0

ClinVar
Risk	rs786204108(C;C)
Alt	rs786204108(C;C)
Reference	Rs786204108(G;G)
Significance	Probable-Pathogenic
Disease	Hemochromatosis type 1
Variation	info
Gene	TFR2
CLNDBN	Hemochromatosis type 1
Reversed	1
HGVS	NC_000007.13:g.100224489C>G
CLNSRC
CLNACC	RCV000168040.1,