rs853326

Orientation

minus

Stabilized

minus

Make rs853326(C;C)

Make rs853326(C;T)

Make rs853326(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

132897729

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs853326
dbSNP (classic)	rs853326
ClinGen	rs853326
ebi	rs853326
HLI	rs853326
Exac	rs853326
Gnomad	rs853326
Varsome	rs853326
LitVar	rs853326
Map	rs853326
PheGenI	rs853326
Biobank	rs853326
1000 genomes	rs853326
hgdp	rs853326
ensembl	rs853326
geneview	rs853326
scholar	rs853326
google	rs853326
pharmgkb	rs853326
gwascentral	rs853326
openSNP	rs853326
23andMe	rs853326
SNPshot	rs853326
SNPdbe	rs853326
MSV3d	rs853326
GWAS Ctlg	rs853326

GMAF

0.3641

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

OMIM	188450
Desc
Variant	0010
Related	also

ClinVar
Risk	rs853326(C;C)
Alt	rs853326(C;C)
Reference	rs853326(T;T)
Significance	Other
Disease	Autoimmune thyroid disease 3 not specified Thyroid dyshormonogenesis
Variation	info
Gene	TG
CLNDBN	Autoimmune thyroid disease 3 not specified Thyroid dyshormonogenesis
Reversed	1
HGVS	NC_000008.10:g.133909974A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013535.3, RCV000254213.1, RCV000368266.1,