rs2071403

Orientation

plus

Stabilized

plus

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

Make rs2071403(A;G)

Make rs2071403(G;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

1413472

Gene

TPO

is a	snp
is	mentioned by
dbSNP	rs2071403
dbSNP (classic)	rs2071403
ClinGen	rs2071403
ebi	rs2071403
HLI	rs2071403
Exac	rs2071403
Gnomad	rs2071403
Varsome	rs2071403
LitVar	rs2071403
Map	rs2071403
PheGenI	rs2071403
Biobank	rs2071403
1000 genomes	rs2071403
hgdp	rs2071403
ensembl	rs2071403
geneview	rs2071403
scholar	rs2071403
google	rs2071403
pharmgkb	rs2071403
gwascentral	rs2071403
openSNP	rs2071403
23andMe	rs2071403
SNPshot	rs2071403
SNPdbe	rs2071403
MSV3d	rs2071403
GWAS Ctlg	rs2071403

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 24722205]
Trait	Anti-thyroid peroxidase antibody positivity
Title	A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.
Risk Allele
P-val	1E-10
Odds Ratio	1.65 [1.50-1.80]

ClinVar
Risk	rs2071403(G;G)
Alt	rs2071403(G;G)
Reference	Rs2071403(A;A)
Significance	Probable-non-pathogenic
Disease	Congenital hypothyroidism
Variation	info
Gene	TPO LOC101927426
CLNDBN	Congenital hypothyroidism
Reversed	0
HGVS	NC_000002.11:g.1417244A>G
CLNSRC
CLNACC	RCV000326086.1,