rs2069561

Orientation

plus

Stabilized

plus

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

Make rs2069561(A;A)

Make rs2069561(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

132963038

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs2069561
dbSNP (classic)	rs2069561
ClinGen	rs2069561
ebi	rs2069561
HLI	rs2069561
Exac	rs2069561
Gnomad	rs2069561
Varsome	rs2069561
LitVar	rs2069561
Map	rs2069561
PheGenI	rs2069561
Biobank	rs2069561
1000 genomes	rs2069561
hgdp	rs2069561
ensembl	rs2069561
geneview	rs2069561
scholar	rs2069561
google	rs2069561
pharmgkb	rs2069561
gwascentral	rs2069561
openSNP	rs2069561
23andMe	rs2069561
SNPshot	rs2069561
SNPdbe	rs2069561
MSV3d	rs2069561
GWAS Ctlg	rs2069561

GMAF

0.3678

Max Magnitude

0

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

ClinVar
Risk	rs2069561(A;A)
Alt	rs2069561(A;A)
Reference	Rs2069561(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Thyroid dyshormonogenesis
Variation	info
Gene	TG
CLNDBN	not specified Thyroid dyshormonogenesis
Reversed	0
HGVS	NC_000008.10:g.133975283G>A
CLNSRC
CLNACC	RCV000242253.1, RCV000305066.1,