rs121908087

Orientation

plus

Stabilized

plus

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

Make rs121908087(C;T)

Make rs121908087(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

1496059

Gene

TPO

is a	snp
is	mentioned by
dbSNP	rs121908087
dbSNP (classic)	rs121908087
ClinGen	rs121908087
ebi	rs121908087
HLI	rs121908087
Exac	rs121908087
Gnomad	rs121908087
Varsome	rs121908087
LitVar	rs121908087
Map	rs121908087
PheGenI	rs121908087
Biobank	rs121908087
1000 genomes	rs121908087
hgdp	rs121908087
ensembl	rs121908087
geneview	rs121908087
scholar	rs121908087
google	rs121908087
pharmgkb	rs121908087
gwascentral	rs121908087
openSNP	rs121908087
23andMe	rs121908087
SNPshot	rs121908087
SNPdbe	rs121908087
MSV3d	rs121908087
GWAS Ctlg	rs121908087

Max Magnitude

0

OMIM	606765
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121908087(T;T)
Alt	rs121908087(T;T)
Reference	Rs121908087(C;C)
Significance	Pathogenic
Disease	Deficiency of iodide peroxidase
Variation	info
Gene	TPO
CLNDBN	Deficiency of iodide peroxidase
Reversed	0
HGVS	NC_000002.11:g.1499831C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004266.3,