rs774274702

Orientation

plus

Stabilized

plus

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

Make rs774274702(A;A)

Make rs774274702(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

132873226

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs774274702
dbSNP (classic)	rs774274702
ClinGen	rs774274702
ebi	rs774274702
HLI	rs774274702
Exac	rs774274702
Gnomad	rs774274702
Varsome	rs774274702
LitVar	rs774274702
Map	rs774274702
PheGenI	rs774274702
Biobank	rs774274702
1000 genomes	rs774274702
hgdp	rs774274702
ensembl	rs774274702
geneview	rs774274702
scholar	rs774274702
google	rs774274702
pharmgkb	rs774274702
gwascentral	rs774274702
openSNP	rs774274702
23andMe	rs774274702
SNPshot	rs774274702
SNPdbe	rs774274702
MSV3d	rs774274702
GWAS Ctlg	rs774274702

Max Magnitude

0

ClinVar
Risk	rs774274702(A;A)
Alt	rs774274702(A;A)
Reference	Rs774274702(G;G)
Significance	Pathogenic
Disease	Iodotyrosyl coupling defect Thyroid dyshormonogenesis
Variation	info
Gene	TG
CLNDBN	Iodotyrosyl coupling defect Thyroid dyshormonogenesis
Reversed	0
HGVS	NC_000008.10:g.133885471G>A
CLNSRC
CLNACC	RCV000207481.1, RCV000272586.1,