rs16904774

Orientation

plus

Stabilized

plus

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

Make rs16904774(A;A)

Make rs16904774(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

132888250

Gene

TG

is a	snp
is	mentioned by
dbSNP	rs16904774
dbSNP (classic)	rs16904774
ClinGen	rs16904774
ebi	rs16904774
HLI	rs16904774
Exac	rs16904774
Gnomad	rs16904774
Varsome	rs16904774
LitVar	rs16904774
Map	rs16904774
PheGenI	rs16904774
Biobank	rs16904774
1000 genomes	rs16904774
hgdp	rs16904774
ensembl	rs16904774
geneview	rs16904774
scholar	rs16904774
google	rs16904774
pharmgkb	rs16904774
gwascentral	rs16904774
openSNP	rs16904774
23andMe	rs16904774
SNPshot	rs16904774
SNPdbe	rs16904774
MSV3d	rs16904774
GWAS Ctlg	rs16904774

Max Magnitude

0

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

ClinVar
Risk	rs16904774(A;A) rs16904774(T;T)
Alt	rs16904774(A;A) rs16904774(T;T)
Reference	Rs16904774(G;G)
Significance	Pathogenic
Disease	Thyroid dyshormonogenesis not provided
Variation	info
Gene	TG
CLNDBN	Thyroid dyshormonogenesis not provided
Reversed	0
HGVS	NC_000008.10:g.133900495G>A; NC_000008.10:g.133900495G>T
CLNSRC
CLNACC	RCV000388671.1, RCV000412820.1,