rs121918678

Orientation

plus

Stabilized

plus

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

Make rs121918678(A;G)

Make rs121918678(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

133777112

Gene

TF

is a	snp
is	mentioned by
dbSNP	rs121918678
dbSNP (classic)	rs121918678
ClinGen	rs121918678
ebi	rs121918678
HLI	rs121918678
Exac	rs121918678
Gnomad	rs121918678
Varsome	rs121918678
LitVar	rs121918678
Map	rs121918678
PheGenI	rs121918678
Biobank	rs121918678
1000 genomes	rs121918678
hgdp	rs121918678
ensembl	rs121918678
geneview	rs121918678
scholar	rs121918678
google	rs121918678
pharmgkb	rs121918678
gwascentral	rs121918678
openSNP	rs121918678
23andMe	rs121918678
SNPshot	rs121918678
SNPdbe	rs121918678
MSV3d	rs121918678
GWAS Ctlg	rs121918678

Max Magnitude

0

OMIM	190000
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121918678(G;G)
Alt	rs121918678(G;G)
Reference	Rs121918678(A;A)
Significance	Pathogenic
Disease	Transferrin variant bv
Variation	info
Gene	TF
CLNDBN	Transferrin variant bv
Reversed	0
HGVS	NC_000003.11:g.133495956A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013453.17,