rs121918676

Orientation

plus

Stabilized

plus

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

Make rs121918676(A;A)

Make rs121918676(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

133756969

Gene

TF

is a	snp
is	mentioned by
dbSNP	rs121918676
dbSNP (classic)	rs121918676
ClinGen	rs121918676
ebi	rs121918676
HLI	rs121918676
Exac	rs121918676
Gnomad	rs121918676
Varsome	rs121918676
LitVar	rs121918676
Map	rs121918676
PheGenI	rs121918676
Biobank	rs121918676
1000 genomes	rs121918676
hgdp	rs121918676
ensembl	rs121918676
geneview	rs121918676
scholar	rs121918676
google	rs121918676
pharmgkb	rs121918676
gwascentral	rs121918676
openSNP	rs121918676
23andMe	rs121918676
SNPshot	rs121918676
SNPdbe	rs121918676
MSV3d	rs121918676
GWAS Ctlg	rs121918676

Max Magnitude

0

OMIM	190000
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918676(A;A)
Alt	rs121918676(A;A)
Reference	Rs121918676(G;G)
Significance	Pathogenic
Disease	Transferrin variant d1
Variation	info
Gene	TF
CLNDBN	Transferrin variant d1
Reversed	0
HGVS	NC_000003.11:g.133475813G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013448.24,