rs121908088

Orientation

plus

Stabilized

plus

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

Make rs121908088(C;G)

Make rs121908088(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

1494011

Gene

TPO

is a	snp
is	mentioned by
dbSNP	rs121908088
dbSNP (classic)	rs121908088
ClinGen	rs121908088
ebi	rs121908088
HLI	rs121908088
Exac	rs121908088
Gnomad	rs121908088
Varsome	rs121908088
LitVar	rs121908088
Map	rs121908088
PheGenI	rs121908088
Biobank	rs121908088
1000 genomes	rs121908088
hgdp	rs121908088
ensembl	rs121908088
geneview	rs121908088
scholar	rs121908088
google	rs121908088
pharmgkb	rs121908088
gwascentral	rs121908088
openSNP	rs121908088
23andMe	rs121908088
SNPshot	rs121908088
SNPdbe	rs121908088
MSV3d	rs121908088
GWAS Ctlg	rs121908088

GMAF

0.0004591

Max Magnitude

0

OMIM	606765
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121908088(G;G)
Alt	rs121908088(G;G)
Reference	Rs121908088(C;C)
Significance	Pathogenic
Disease	Deficiency of iodide peroxidase not provided
Variation	info
Gene	TPO
CLNDBN	Deficiency of iodide peroxidase not provided
Reversed	0
HGVS	NC_000002.11:g.1497783C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004268.3, RCV000440090.1,