rs104893669

Orientation

plus

Stabilized

plus

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

Make rs104893669(A;T)

Make rs104893669(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

1484596

Gene

TPO

is a	snp
is	mentioned by
dbSNP	rs104893669
dbSNP (classic)	rs104893669
ClinGen	rs104893669
ebi	rs104893669
HLI	rs104893669
Exac	rs104893669
Gnomad	rs104893669
Varsome	rs104893669
LitVar	rs104893669
Map	rs104893669
PheGenI	rs104893669
Biobank	rs104893669
1000 genomes	rs104893669
hgdp	rs104893669
ensembl	rs104893669
geneview	rs104893669
scholar	rs104893669
google	rs104893669
pharmgkb	rs104893669
gwascentral	rs104893669
openSNP	rs104893669
23andMe	rs104893669
SNPshot	rs104893669
SNPdbe	rs104893669
MSV3d	rs104893669
GWAS Ctlg	rs104893669

Max Magnitude

0

OMIM	606765
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104893669(G;G) rs104893669(T;T)
Alt	rs104893669(G;G) rs104893669(T;T)
Reference	Rs104893669(A;A)
Significance	Pathogenic
Disease	Deficiency of iodide peroxidase
Variation	info
Gene	TPO
CLNDBN	Deficiency of iodide peroxidase
Reversed	0
HGVS	NC_000002.11:g.1488368A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004258.2,